We are Sila—a next generation battery materials company dedicated to accelerating energy transformation for a more sustainable future. 

Our next-gen anode material is the first significant chemistry improvement to lithium-ion batteries to reach the market in 30 years. Our silicon anode material is a simple drop-in replacement to graphite and significantly boosts the energy density of lithium-ion batteries without compromising performance. 

Today, Sila science powers innovative consumer electronics. Tomorrow, it will fuel our EV future and the electrification of everything. 

We work directly with leading consumer electronics and automotive OEMs to help accelerate product roadmaps, and partners with battery manufacturers commercial cell production. Our partners include BMW, Daimler, and ATL.

Sila Nano’s first products significantly increase the energy density of state-of-the-art lithium-ion batteries. Our materials are manufacturable economically at scale and are drop-in replacements to existing battery manufacturing processes.

Industry: Climate Technology Product Manufacturing
Company Size: 201-500 employees

Sila Nanotechnologies, Inc.

Savvy Admin PROD

**About Us **We are Sila, a next-generation battery materials company. Our mission is to power the world’s transition to clean energy. To create this future, our team is building a better lithium-ion battery from the inside out today. We engineer and manufacture ground-breaking battery materials that significantly increase the energy density of batteries, while reducing their size and weight. The result? Smaller more powerful batteries that can unlock innovation in consumer devices and accelerate the mass adoption of electric cars to eliminate our dependence on fossil fuels. We're tackling one of the biggest challenges of our time every day, and together we're redefining what's possible. Are you ready to be a part of a team committed to changing the world?

Who You AreAs a Staff Scientist on the Analytics Team, you are a creative, collaborative, and hands-on analytical scientist with extensive experience in developing and validating analytical methods on a variety of instruments. You are passionate and knowledgeable about analytical chemistry, material characterization, process control, or related topics. You approach complex technical problems with curiosity, persistence, and high standards. You pride yourself on being resourceful and independent, able to effectively manage multiple projects and deliver results on time in a fast-paced environment with constantly evolving information. You know how to be a thoughtful, supportive team member, ready to give and receive feedback with humility.

Responsibilities and Duties

Independently scope, plan, and execute complex analytical development projects involving multiple stakeholders to expand Sila’s measurement capabilities for both R&D and QC. Specifically:

- Identify and propose solutions that best meet business and technical needs, ensuring cross-functional alignment with engineers and management

- Evaluate, select, procure and install analytical instrumentation as necessary.

- Establish best practices in sample preparation, instrumental analysis, data analysis, and result reporting.

- Write Standard Operating Procedures (SOPs), train team members, and conduct rigorous Measurement System Analyses (MSA).

- Prepare validation reports and present technical data to engineering and quality teams.

Knowledge and Skill Requirements

- Degree in Chemistry, Physics, Material Science, Chemical Engineering, or equivalent with a minimum of 8 years (Bachelor’s degree), 5 years (Master’s degree), or 3 years (PhD) of industry experience in analytical method development.

- Experience in analytical method development through all phases of maturity, from ideation to implementation and validation. Must be well versed in concepts of Precision, Accuracy, Linearity, Robustness, etc.

- Experience with quantitative analysis and statistical tools like ANOVA, Gage R&R, SPC, etc. Experience with JMP is a plus.

- Expertise in several relevant analytical techniques such as laser particle size analysis (LPSA), Raman spectroscopy, BET gas adsorption analysis, density analysis (bulk, tap, envelope, skeletal, true), TGA, ICP, XRF, SEM-EDS, XRD, dynamic image analysis, gas chromatography, and others.

- Excellent oral and written communication skills; able to convey complex information effectively to diverse audiences

- Self-motivated, resourceful, and independent; able to manage multiple responsibilities with minimal supervision

- (Preferred) Experience in highly regulated laboratories and production environments (FDA, AIAG, VDA, ISO 17025).

- (Preferred) Experience with proper sampling of powder and granular materials.

Physical Demands and Working Conditions

- Operate a computer and other office equipment, such as a laptop, copier/printer, etc in a fixed location

- Precise and repetitive use of hands - light to forceful handling of a range of material quantities.

- Wear personal protective equipment including, but not limited to, a lab coat, gloves, safety glasses, and steel toe safety shoes.

- Pass a respirator fit test and be able to wear respiratory protection.

The starting base pay for this role is between $151,000 and $191,000 at the time of posting. The actual base pay depends on many factors, such as education, experience, and skills. Base pay is only one part of Sila’s competitive Total Rewards package that can include benefits, perks, and equity. The base pay range is subject to change and may be modified in the future.

**Working at Sila **We believe that building a diverse team at Sila helps us amplify our individual talents. We are an equal opportunity employer and committed to creating an inclusive environment where good ideas are free to come from anyone. We are proud to celebrate diversity and all qualified applicants are considered for employment without regard to gender, race, sexual orientation, religion, age, disability, national origin, or any other status protected by law.

Staff Scientist, Analytical Development

At Merck, known as MSD outside of the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.merck.com. 

This site is intended for residents of the United States and Canada and their territories only. FLS: http://merck.us/3TKXNuZ

Industry: Pharmaceutical Manufacturing
Company Size: 10,001+ employees

Merck

**Job Description**

**Job Location:**

West Point, PA

The Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) is seeking a bioanalytical scientist to join our Regulated PK & ADA Bioanalytical group at West Point, PA. We are looking for a highly motivated candidate with experience in advanced analytical method design through the use of automation and operational support of bioanalytical labs conducting bioanalysis of biotherapeutics in regulated drug development studies. Collaboration, innovation, teamwork, and accountability are highly valued within our team. The successful candidate will play a key role in designing, planning, and utilizing automation methods during method development, validation, and sample analysis of bioanalytical assays for our Company's pipeline.

**Main Responsibilities Include But Are Not Limited To**

- Assist in establishing and managing bioanalytical lab operations, including lab automation, analytical instrumentation, and data handling.

- Contribute to the development, validation and implementation of novel automated workflows.

- Work collaboratively with department members to operate and troubleshoot automated laboratory equipment and systems in support of various bioanalytical assays within our Company's pipeline.

- Manage data integrity through automated processes.

- Support timely delivery of high-quality quantitative data to cross-functional collaborators for bioanalytical analysis.

- Collaborate to identify, evaluate, and recommend novel and cutting-edge automation and assay strategies to drive our development programs, including machine learning and artificial intelligence.

**Education Minimum Requirements**

- B.A./B.S. in Engineering, Automated Sciences, Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline with a minimum of 3 years of relevant experience.

- Master’s Degree with 1 to 3 years of relevant experience

**Required Experience And Skills**

- Demonstrated expertise operating various automation platforms (e.g. Hamilton, Tecan, Biomek) to perform method development and sample testing of preclinical and clinical assays

- Experience in development and execution of quantitative and qualitative bioanalytical assays (e.g. ELISA, mass spectrometry)

- Knowledge of GLP requirements and understanding of current industry trends and regulatory expectations associated with bioanalytical science.

- Knowledge and experience with data visualization tools (i.e. PowerBI, Spotfire, etc.)

- Strong verbal and written communication skills

- Experience in good documentation practices.

- Self-starter with ability to work independently.

- Ability to follow procedures and thoroughly document experiments.

- Capable of working efficiently and multitasking in a fast-paced environment

- Ability to re-prioritize workload to support team based on immediate need

- Emphasizes a team-based approach and is dedicated to collaborative and harmonious work with others.

**Preferred Experience And Skills**

- Experience with computer languages and building applications (e.g. VB, Python, C#, labview, Microsoft PowerApps)

- Previous work experience in regulated industry environment and a solid understanding of current GLP standards

**Required Skills**

Bioanalysis, Biochemistry, Data Analysis, Data Visualization, Detail-Oriented, Drug Metabolism, Ethical Compliance, GMP Documentation, Good Laboratory Practices (GLPs), Immunoassays, Ligand Binding Assay, Liquid Chromatography-Mass Spectrometry (LC-MS), Pharmacokinetics

**Preferred Skills**

Analytical Instrumentation, Automated Liquid Handling Systems, Biochemistry Techniques, Biological Analysis, C# Automation, LabVIEW(Laboratory Virtual Instrument Engineering Workbench), Microsoft Power Apps, Programming Languages, Python (Programming Language)

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

**Requirements**

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$87,300.00 - $137,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

**San Francisco Residents Only: ** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

**Los Angeles Residents Only: ** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

**Search Firm Representatives Please Read Carefully**

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

N/A

**Job Posting End Date**

04/24/2026

- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

**Requisition ID: **R392976

Scientist, Pharmacokinetics

Wiley’s leading media brand providing first-hand information on the global chemical, life science and process industries

Industry: Zeitungsverlage
Company Size: 201–500 Beschäftigte

CHEManager International

**Company Description**

**About Syngenta**

At Syngenta Crop Protection, we're pioneering solutions that safeguard global food security while championing sustainable agriculture. As a world market leader headquartered in Switzerland, we empower farmers with innovative crop protection technologies that defend against nature's toughest challenges. We unite advanced science with digital solutions to develop intelligent crop protection that maximizes yields while minimizing environmental impact. Join our mission of revolutionizing plant protection from seed to harvest.

**Job Description**

At Syngenta, our goal is to build the most collaborative and trustworthy team in agriculture, providing top-quality seeds and innovative crop protection solutions that improve farmers' success. To support this mission, Syngenta's Research Chemistry Team is seeking an Analytical Scientist in Greensboro, NC. This role will support Product Chemistry Formulation (PCF) projects to enable product registrations in countries outside of North America.

The Analytical Scientist will perform a wide variety of physical properties analyses (e.g. wet chemistry) on chemical pesticides and biological pesticides, using internationally recognized physical test methods (e.g. CIPAC, ASTM, etc.). This role also includes chromatographic analyses for active ingredient content (gas chromatography and high-performance liquid chromatography).

The successful candidate will be responsible for generating fully GLP (Good Laboratory Practice) compliant raw data, protocols and reports, for submission to regulatory authorities as part of new product development projects, regulatory data call-ins, etc. This role is expected to work independently on daily tasks, while contributing to the delivery of each project as part of a highly collaborative team environment.

**Accountabilities**

- Perform physical properties testing and active ingredient content analysis of formulated products accurately, with minimal supervision.

- Strictly adhere to GLP (Good Laboratory Practice) regulatory standards independently, throughout all lab related activities.

- Develop expertise in a wide variety of internationally recognized analytical methods (e.g. CIPAC methods, etc.), strictly adhering to these methodologies.

- Organize raw data into GLP compliant raw data packets / dossiers and generate high-quality study reports.

- Develop proficiency with computer/software platforms such as Microsoft Office software, Chromeleon chromatography software, StarLims, and various other internal platforms.

- Ensure effective problem solving and independent follow-up when unexpected situations arise during testing (e.g. unanticipated test results, etc.).

- Provide consistent, proactive and effective communication within the team, with project stakeholders, data requestors, etc.

**Qualifications**

**Required:**

- Bachelor's degree in Chemistry or another related field is required.

- A minimum of 1-3 years' laboratory experience is required with a Bachelor's degree in Chemistry or other related field.

- Chromatography experience (i.e. HPLC and GC) is preferred.

- Physical properties testing experience (i.e. wet chemistry) is preferred.

- Deliver high quality analytical data on-time, data interpretation and problem solving for product development projects.

- Ability to communicate effectively and efficiently with department members, internal regulatory customers, and project stakeholders to present data, outline challenges and propose solutions.

- Ability to critically inspect and proofread their own data and documents, and those of their colleagues, to proactively find and correct any issues.

- Multi-tasking is required, as activities and testing can vary from day-to-day, depending on project scope.

**Desired**

- Maintain meticulous attention to detail and accurate recordkeeping.

- Demonstrate strong organizational skills and the ability to manage multiple priorities.

- Communicate clearly and professionally in both written and verbal formats.

- Adapt quickly to new tasks and changing priorities, as business needs require.

- Resolve issues proactively by identifying challenges early and implementing timely solutions.

- Execute assigned work independently while collaborating effectively within a flexible, team-based environment.

- Train and guide contractor work activities, as needed, to support project execution.

**Additional Information**

**What We Offer:**

- A culture that celebrates belonging and collaboration, promotes professional development and strives for a work-life balance that supports the team members. Offers flexible work options to support your work and personal needs.

- Full Benefit Package (Medical, Dental & Vision) that starts your first day.

- 401k plan with company match, Profit Sharing & Retirement Savings Contribution.

- Paid Vacation, Paid Holidays, Maternity and Paternity Leave, Education Assistance, Wellness Programs, Corporate Discounts, among other benefits.

Syngenta has been ranked as a top employer by Science Journal. Learn more about our team and our mission here: https://www.youtube.com/watch?v=OVCN_51GbNI

Syngenta is an Equal Opportunity Employer and does not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.

**WL: 3B**

Analytical Scientist

**Job Description**

**Job Location:**

West Point, PA

The Department of Pharmacokinetics, Dynamics, Metabolism, and Bioanalytics (PDMB) is seeking a bioanalytical scientist to join our End-to-End Regulated PK & ADA Bioanalytical group located at our research and development site in West Point, PA. Experience in the field of quantitative bioanalysis of small molecules and biotherapeutics, leveraging LC-MS/MS and/or ligand binding methods in a regulated drug development environment, is highly preferred. In this position, you will be responsible for developing bioanalytical methods for measuring biotherapeutics, such as small molecules, monoclonal antibodies, proteins, peptides and antibody-drug conjugates in support of Good Laboratory Practice (GLP) and clinical studies.

**Main Responsibilities Include But Are Not Limited To**

- Method development, validation, and sample analysis for the quantitation of drug candidates in biological matrices (e.g., serum, plasma)

- Delivering high quality quantitative data in a timely manner to cross-functional collaborators.

- Effectively documenting, tracking, and communicating scientific findings and recommendations within cross-functional teams

- Contributing to establishing and maintaining bioanalytical lab operations including safety, compliance, automation and analytical instrumentation.

- Contributing to authoring of method development reports, test methods, qualification and validation reports, and study reports.

**Education Minimum Requirements**

- B.A./B.S. in Biology, Immunology, Molecular Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline with a minimum of 3 years of relevant experience

- Master’s Degree in Biology, Immunology, Molecular Biology, Chemistry, Biochemistry, Pharmaceutical Sciences, or related discipline with 1 to 2 years of experience

- undefined

**Required Experience And Skills**

- Knowledge of the basic principles of regulated bioanalysis and Good Laboratory Practice (GLP)

- Good verbal and written communication skills

- Ability to follow procedures and thoroughly document experiments.

- Strong direct experience with LC-MS and/or ligand binding assay methodologies for quantitative and qualitative analysis of biotherapeutics

- Understanding of the drug discovery and/or development process and DMPK science

- Ability to work efficiently and multitask in a fast-paced environment

- Fosters team-based approach to research; committed to working synergistically and harmoniously with others

**Preferred Experience And Skills**

- Experience with antibody drug conjugate (ADC) bioanalysis is advantageous.

- Understanding of immunogenicity and anti-drug antibody method development.

**Required Skills**

Antibody Drug Conjugates (ADC), Bioanalysis, Biochemistry, Data Analysis, Data Visualization, Detail-Oriented, Drug Metabolism, Ethical Compliance, GMP Documentation, Good Laboratory Practices (GLPs), Immunoassays, Immunochemistry, Immunology, Immunotherapy, Ligand Binding Assay, Liquid Chromatography-Mass Spectrometry (LC-MS), Molecular Biology, Pharmacodynamics, Pharmacognosy, Pharmacokinetics, Pharmacotherapeutics, Sample Analysis, Small Molecule Screening

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

**Requirements**

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$87,300.00 - $137,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

**San Francisco Residents Only: ** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

**Los Angeles Residents Only: ** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

**Search Firm Representatives Please Read Carefully**

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

No

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

N/A

**Job Posting End Date**

04/23/2026

- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

**Requisition ID: **R393012

Amneal Pharmaceuticals, Inc. (NASDAQ: AMRX) is guided by a simple belief: essential medicines should be accessible to everyone. What began as a promise to deliver high-quality, affordable medicines has evolved into a diversified portfolio spanning complex generics and injectables, biosimilars, and specialty medicines, including more than 290 products, with scale and capabilities that help reach patients across the healthcare system while combining world-class precision with a deep sense of personal responsibility for every dose we deliver. 

Content is for informational purposes only and 3rd party content does not reflect Amneal’s opinions. 

Amneal has the right to remove comments that violate another’s copyright or intellectual property, mention an Amneal product, use profanity or are defamatory, promote and solicit for third-party sites, initiatives, or products, or are factually inaccurate or misleading or spam. 

Amneal recommends that you consult with your healthcare provider regarding personal health matters. To report a product complaint or adverse event related to an Amneal product, contact Drug Safety at 877-835-5472, option 3 or drugsafety@amneal.com. If you are currently experiencing a life-threatening event, please immediately contact 911.

Industry: Pharmaceutical Manufacturing
Company Size: 5,001-10,000 employees

Amneal Pharmaceuticals

**Job Description**

**Description:**

The Scientist-2 is a mid-level analytical scientist opportunity supporting the analytical development of pharmaceutical oral dosage form. The individual in this capacity performs analytical methods qualifications/validations, analyzes active pharmaceutical ingredients, excipients, and finished dosage forms using appropriate analytical methods and maintains/qualifies analytical equipment.

**Essential Functions:**

- Performs analysis and release of active pharmaceutical ingredients, excipients, in-process materials, and finished drug products to support the formulation development team, maintaining full compliance with all applicable US FDA - cGMP regulations and internal SOPs.

- Develops and optimizes new and existing analytical methods for qualification and release testing of products. Develops stability indicating methods and performs methods validation.

- Provides timely responses to all internal and external inquiries.

- Ensures deadlines are met for product development schedules, and checks that technical and compliance requirements are met.

- Evaluates, recommends, and implements new analytical technologies and instrumentation for testing.

- Assists with training other members of the analytical development team.

**Additional Responsibilities:**

- Stays abreast of new developments in analytical technologies. Contributes to improvement in laboratory operations to increase efficiency and GMP compliance.

**Qualifications**

**Education:**

- Bachelors Degree (BA/BS) Chemistry or related science - Required

- Master Degree (MS/MA) Chemistry or related science - Preferred

**Experience:**

- 3 years or more in pharmaceutical experience (with Bachelor's Degree)

- 1 year or more in pharmaceutical experience (with Master's Degree)

**Skills:**

- Enthusiasm and dedication to learn and adopt new analytical techniques. - Intermediate

- Written and verbal communication and presentation skills. - Intermediate

- Ability to set priorities and to follow through on commitments utilizing organizational skills. - Intermediate

- Microsoft Office and ability to learn additional software/programs as needed. - Intermediate

- Meet deadlines under pressure. - Intermediate

- Able to work in a team environment. - Intermediate

- Creativity to solve technical and compliance problems. - Intermediate

**Specialized Knowledge:**

- Broad knowledge of modern analytical equipment and techniques.

- Extensive experience in cGMP laboratory testing. Hands-on experience with HPLC, GC, TLC, and MS.

- Methods development experience.

- Experience writing the standard operating procedures (SOPs) and test methods.

The base salary for this position ranges from $80,000 to $90,000 per year. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, with this position within the first 12 months. Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.

**About Us**

Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws.

Inhalation Scientist, Analytical R&D

**About Ingredion:**

Join Ingredion, where innovation impacts lives worldwide! Without even realizing it, you've experienced our work in your favorite chocolate, your pet's food, the paper you write on, and your everyday snacks. As a global powerhouse across more than 60 industries, we harness the potential of natural ingredients to transform lives. Whether you're just starting your career or bringing years of experience, there's a place for you here to make a real difference. Be part of our team that values a wide range of perspectives and is committed to shaping a better world with every product we create.

Workplace type: On Site (with flexibility to work from home on Fridays)

As a **Senior ** **Analytical Scientist **, you will lead analytical initiatives, overseeing research experiments, ensuring data integrity, and providing analytical support for new solutions, raw material qualifications, and manufacturing processes.

This role reports to the Sr. Manager, Application and development, Customized solutions US/CAN

**What You Will Do:**

- Build analytical capability to support microdosed customized solutions and hydrocolloid ingredients.

- Interpret and report analytical data to support formulation development, stability studies, and product specification/release.

- Collaborate with cross-functional teams including R&D, Quality, Regulatory, and Manufacturing to support fast-track commercialization projects by developing new testing methods and specification.

- Develop, validate, and execute analytical testing methods for new systems and perform routine and non-routine testing using techniques such as HPLC, GC, FTIR, UV-Vis, and wet chemistry.

- Lead the raw material qualification for hydrocolloids and customized solutions.

- Provide support for contract manufacturing and testing facilities.

- Identify and address capability gaps in knowledge, equipment, and facilities; work with management to resolve these gaps.

- Author and review technical documents including method validation protocols, reports, specifications, and SOPs.

- Troubleshoot and resolve technical problems promptly to prevent project delays.

- Supervise lab technicians, ensuring timely execution and completion of assigned projects.

- Maintain and calibrate all analytical equipment, coordinate with external vendors for repairs, quotes, installation, and service contracts.

- Work independently on long-term project assignments, ensuring timely completion.

- Ensure and maintain a safe, accident-free laboratory environment.

**What You Will Bring:**

- Master's degree in chemistry or food science (or equivalent) with at least 5 years of experience, or PhD with 1-3 years of experience.

- Strong background in analytical science, with the ability to develop testing methods and optimize systems to meet customer needs.

- Hands-on experience in analytical laboratories, including operations of HPLC, GC, FTIR/NIR, and UV-Vis instrumentation.

- Experience and knowledge in hydrocolloids and customized solutions is preferred.

- Understanding of rheology with experience with particle size analyzers, rheometers, texture analyzers, and RVA is highly desirable.

- Demonstrated intellectual leadership through staying current with industry trends and academic developments in relevant technical areas.

- Occasional domestic travel may be required.

**Who You Are:**

- Strong written and verbal communication skills; able to communicate effectively across functional lines and organizational levels.

- Excellent interpersonal skills: thrive in collaborative environments and contribute to team-based solutions.

- Experience with statistical analysis and design of experiments.

**Why Join Ingredion?**

Discover Why Ingredion Is The Ideal Place To Advance Your Career With Our Exceptional Rewards And Benefits Package Designed To Help You Thrive. Create The Future With Us And Enjoy:

- Total Rewards Package - Competitive salary and performance-based pay recognizing your contributions to our success

- Comprehensive Benefits & Wellness Support - Health, long-term savings, and resources for your physical, mental, and emotional well-being

- Career Growth - Learning, training, and development opportunities, including tuition reimbursement

- Employee Recognition Program - A culture of real-time appreciation, with personalized recognition rewards globally

- Employee Discount Program - Provides exclusive discounts on everyday products, services, and travel

We are an equal opportunity employer and value diversity at our company. Ingredion seeks to provide a work environment that is free from harassment and discrimination. We will not tolerate any form of discrimination based on race, color, religion, age, gender, gender identity, gender expression, national origin, ancestry, handicap or disability-mental or physical-marital status, sexual orientation, veteran status, disability resulting from military service, or any other classification protected by law ("protected classifications"). We are committed to establishing and maintaining a work environment where everyone is treated with dignity and respect.

Ingredion provides accommodations to job applicants with disabilities throughout the hiring process. If a job applicant requires an accommodation during the application process or through the selection process, we will work with the applicant to meet the job applicant's accommodation needs.

Ingredion uses AI-enabled tools to support parts of the recruitment process, including resume screening and interview scheduling. These tools help match candidate skills to job requirements and streamline communication. All AI-assisted decisions are reviewed by our Talent Acquisition team to ensure fairness and compliance with applicable laws. By applying, you acknowledge that AI may be used to support your application journey.

**Relocation Available:**

Yes, Within Country

**Pay Range:**

This pay range is not a guarantee of compensation or salary. Final base salary will be determined based on several factors which may include but are not limited to responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data and applicable bargaining agreement (if any).

**Incentive Compensation:**

As a part of the total compensation package, this role may be eligible for the Ingredion Annual Incentive Plan or a role-specific commission/bonus.

**Benefits:**

Full-time roles are eligible for our comprehensive benefits package which includes medical, dental and vision coverage as well as a 401(k) plan with an competitive company match.

Senior Analytical Scientist, Applications and Development, Customized Solutions, US/CAN

Astrix is the unrivaled market-leader in creating & delivering innovative strategies, solutions, and people to the life science community.  

Through world class people, process, and technology, Astrix works with clients to fundamentally improve business & scientific outcomes across many domains including the laboratory, clinical & regulatory, pharmacovigilance, R&D, and manufacturing. 

Founded by scientists to solve the unique challenges of the life science community, Astrix offers a growing array of strategic, application & platform, data transformation & analytics, change management, and staffing services designed to deliver immediate value to clients and solve their most complex technical and staffing challenges.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Astrix

We are seeking a **Quality Control Scientist ** to join the Raw Materials team supporting a global pharmaceutical/biotech organization. This is a great opportunity to gain hands-on experience in a GMP environment with strong potential for long-term growth and conversion.

**Location **: San Diego County, CA (Onsite)

**Pay Rate: ** $36–$47/hr (based on experience)

**Schedule: ** Monday – Friday, 8:00 AM Start

**6-Month Contract **( potential for conversion)

**Pay Rates**

(1–3 years): Up to $36/hr

(3–5 years): Up to $40/hr

(5+ years): Up to $47/hr

**Key Responsibilities**

- Perform QC testing on raw materials, in-process samples, and finished products

- Conduct analytical testing and review data for accuracy and completeness

- Maintain compliance with cGMP standards, SOPs, and documentation practices

- Write, revise, and support GMP documentation (SOPs, specifications, test methods)

- Operate and maintain analytical instrumentation (HPLC, UPLC, GC, Mass Spec, UV)

- Support method validation, calibration, and equipment maintenance

- Manage raw material processes including receiving, quarantine, testing, and release

- Investigate deviations, out-of-specification results, and support stability activities

**Qualifications**

- Bachelor’s degree in Chemistry or related field (Master’s preferred)

- Minimum 1+ year of experience in a GMP pharma/biotech environment

- Hands-on experience with HPLC (required)

- Experience with analytical instrumentation (GC, HPLC, Mass Spec, etc.)

- Experience in QC, raw materials, or analytical lab settings

- Strong understanding of GMP and documentation practices

~~This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!~~

INDBH

Quality Control Scientist

Founded in 2012, Planet Pharma is a global leader in life sciences recruitment and staffing, specializing in Pharmaceuticals, Biotechnology, Medical Device, Labs & Healthcare, Specialty Providers, CMOs / CDMOs, and Contract Research Organizations (CROs). We provide the following solutions: Contract & Direct Hire (Permanent) Staffing, Strategic Resourcing, Retained & Executive Search, Functional Service Provider (FSP), and Global Workforce Solutions.

Planet Pharma has offices throughout North America, Europe, and APAC. All locations operate with shared attributes at the heart of everything we do!

🚨 Job Scam Warning 🚨
We’ve recently been made aware of fraudulent activity where individuals are posing as representatives of Planet Pharma and contacting job seekers using fake email addresses.

✅ All genuine emails from Planet Pharma will always come from an address ending in @planet-pharma.com, @planet-pharma.co.uk, or @ppgadvisorypartners.com.

❌ We will never contact you from free email services or unfamiliar domains.

If you receive a message claiming to be from us and are unsure if it’s legitimate, reach out to us directly at contactus@planet-pharma.com for verification. Your safety and trust are our priority!

Industry: Staffing and Recruiting
Company Size: 1,001-5,000 employees

Planet Pharma

Pay 30-40/h depending on experience

**Purpose**

The QC Scientist I Raw Materials will be responsible for executing and troubleshooting a variety of laboratory test methods, defining the requirements for implementation of procedures, processes and assays within QC, and identifying and implementing continuous improvement initiatives related to overall laboratory functionality. This role will work closely with the assay transfer technical lead. This role will mentor junior analysts and develop and facilitate training initiatives within the labs.

**Essential Job Responsibilities**

- Develop/author/revise technical reports and laboratory procedures (SOPs, methods)

- Execute and troubleshoot raw material testing in support of production activities

- Perform routine release sampling and managing testing of raw materials, such as compendial analysis per USP, Ph.Eur., and JP monographs and general chapters, based on cGMP and internal procedures

- Design and perform testing in support of method transfer/validation/qualification/verification

- Review/authorize data and perform analysis and interpretation of test results and trends

- Design and/or participate in method development; equipment qualification/validation studies; deviation and OOS investigations

- Perform QC lab support activities including but not limited to sample management, reagent preparation, instrumentation maintenance, and instrument calibration

- Support and mentor junior team members

- Collaborate with other network sites to share best practices

- Other duties as required

**Quantitative Dimensions**

The QC Scientist I Raw Materials will be accountable for executing and troubleshooting a variety of laboratory test methods, defining the requirements for implementation of procedures, processes and assays within QC, and identifying and implementing continuous improvement initiatives related to overall laboratory functionality.

**Organizational Context**

The QC Scientist I Raw Materials will typically report to the Senior Manager, Quality Control Raw Materials. This role is expected to Model our Core Values and to demonstrate work performance as someone who exemplifies the culture we want to create; operates with transparency; is trusted; and supports the overall mission and vision of Gene Therapies and the organization

**Qualifications**

Required:

- B.S. degree in chemistry, biological sciences or related field with 6+ years or M.S. degree with 4+ years of relevant experience in a GMP Quality Control role

- Prior laboratory hands-on experience with a variety of techniques such as FTIR, Raman, Near-IR, HPLC analysis and other compendial assays

- Technical knowledge and experience in relevant areas of 21CFR, ICH, USP, Ph. Eur. and FDA guidance documents as well as cGXPs in support of clinical and commercial manufacturing

- Proven knowledge in cGMP raw material program (RM sampling plans and testing requirements)

- Ensures inspection, testing and release timelines are met.

- Strong understanding of data integrity requirements and regulatory requirements pertaining to biotechnology and pharmaceutical industries and proven experience analyzing experimental data

- Experience using LIMS as an end user; Excellent technical writing and verbal communication skills

- Must be capable of observing and adhering to lab safety standards and procedures

- Successfully performs work independently with minimal instructions

- Strong interpersonal skills, highly collaborative within a multi-discipline team and contributes to a supportive and positive work environment, strong knowledge of GMP, SOPs and quality control processes, and strong knowledge of quality systems and regulatory requirements

- Excels in a fast-paced team environment, handles multiple tasks concurrently, and in a timely fashion

- Highly self-motivated and goal oriented

- Will support and demonstrate quality standards to ensure data of highest quality and works closely with team and other functional key stakeholders on the Operations team to execute work and will be expected to perform other duties and/or special projects as assigned

**Preferred:**

- Experience in a Biotech/Pharmaceutical company with a high growth, fast-paced environment

- Experience in qualification of analytical equipment, including those with computerized systems

- Experience in method validation/qualification/verification/transfer

**Working Conditions:**

- This role frequently requires long periods of sitting, standing and use of hands and regular motion to include bending, stooping, and lifting up to 20lbs.

- This is an on-site role working in a cGMP regulated manufacturing facility.

Responsibilities:• Supports global laboratories with ongoing projects related to Laboratory Information Management Systems (LIMS), in particular Thermo SampleManager.

• Works with Global Quality Systems support team on creating and routing document change controls including administrative updates to procedures and training.

• Works with global and site resources to manage requests related to inventory management.

• Assists with global digital readiness preparation and other project activities on an as needed basis.

• Willingness to learn and provide support

Desired experience:• Lab administration, supporting quality systems used by the laboratory, especially LIMS such as SampleManager.

• Laboratory analyst with chromatography experience is a plus but not required.

• Scientific background with experience following analytical test methods.

• Multi-site or multi-stakeholder project work supporting laboratory quality systems.

*CO/NYC candidates might not be considered

Remote Lab Technician

Pharmaron: Global Life Sciences Services Provider
Stock Code: 300759.SZ/3759.HK

Founded in 2004, Pharmaron is a premier life sciences service provider that offers a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. 

Pharmaron’s Comprehensive CRO & CDMO Services 
•	Synthetic, Medicinal, and Analytical Chemistry Services
•	Biology Services (e.g., in vitro screening, structural biology, biomarkers)
•	DMPK Services (e.g., in vitro ADME, in vivo PK, PKPD, mass balance)
•	Pharmacology Services (e.g., in vivo pharmacology, animal disease models, immunotoxicity)
•	Drug Safety Assessment Services (e.g., toxicology, safety pharmacology, genetic toxicology)
•	Radiochemistry and Isotopically Labelled Metabolism Services (e.g., 14C/Carbon-14 radiosynthesis, 3H/tritium radiosynthesis, QWBA, mARG)
•	CMC Services (e.g., API manufacturing, process chemistry, formulation development)
•	Clinical Development Services (e.g., First-in-Human [FIH], ethnobridging, microdosing Phase 0, absolute bioavailability)

Commitment to Excellence and Innovation

With a proven track record of success, Pharmaron continually invests in its people, facilities, and technologies to meet evolving scientific and regulatory demands. The company prides itself on enabling scientific breakthroughs and supporting its partners in advancing human health.
_

Learn More:  Explore Pharmaron’s services to discover how to accelerate your R&D programs. www.pharmaron.com.

_

Keywords:  CRO, CDMO, synthetic chemistry, medicinal chemistry, biology, radiochemistry, toxicology, First-in-Human, API manufacturing, PKPD, 14C radiosynthesis, discovery biologics, clinical development, small molecules, biologics, cell and gene therapy (CGT) products

Industry: 制药业
Company Size: 超过 10,001 人

Pharmaron

**Position **: Senior Scientist – Analytical Chemistry

**Salary Range: **$90k - $130k

**Location: **Coventry, RI

**About Pharmaron**

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 21,000 employees worldwide across 23 locations in the US, UK and China, we support drug discovery through to manufacturing with fully integrated, high-quality services.

We're proud of the impact we make and just last year, we supported over **780 discovery projects **, **1,000+ CMC programmes **, and **1,000+ clinical trials **across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than **3,000 global customers **. To learn more, visit www.pharmaron.com.

**Job Overview**

The Senior Scientist - Analytical Chemistry will serve as a key technical resource within the Quality Control laboratory supporting API manufacturing and development programs at Pharmaron's Coventry, RI facility.

This role is responsible for supporting analytical method validation, transfer, troubleshooting, and QC testing of raw materials, intermediates, and active pharmaceutical ingredients in a cGMP-regulated laboratory environment. The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations.

**Key Responsibilities**

- Support analytical method validation, verification, and transfer activities within the QC laboratory.

- Troubleshoot complex analytical challenges related to API characterization and GMP testing.

- Review analytical data, laboratory notebooks, and instrument qualification documentation to ensure scientific accuracy and regulatory compliance.

- Lead or support laboratory investigations, deviations, and root cause analyses.

- Maintain laboratory equipment and serve as system owner for analytical instrumentation, including qualification and maintenance activities.

- Provide technical mentorship and scientific guidance to QC scientists and laboratory personnel.

- Prepare and revise standard operating procedures (SOPs), analytical methods, and technical documentation.

- Support internal and external regulatory inspections and client audits as an analytical subject matter expert.

- Collaborate with cross-functional teams including Manufacturing, Process Chemistry, Quality Assurance, and Regulatory Affairs.

- Contribute to continuous improvement initiatives that enhance QC laboratory efficiency and analytical capabilities.

- Perform other related assignments and duties, as required and assigned.

**What We're Looking For**

- Ph.D. in Chemistry or a related field with 1–4 years of postdoctoral or industry experience.

- MS with 5–8 years of pharmaceutical industry experience, BS with 7–10 years of relevant pharmaceutical industry experience

- 3 years of experience (may include Ph.D. experience) with core analytical instrumentation such as HPLC, GC, FTIR, UV, Mass Spectrometry.

- Demonstrated experience applying analytical techniques to solve complex scientific problems related to method validation, troubleshooting, and implementation

- Strong hands-on expertise with analytical instrumentation including:

- HPLC / UPLC

- GC

- FTIR

- UV

- Mass Spectrometry

- Experience supporting API manufacturing or pharmaceutical QC laboratories

- Proven ability to troubleshoot analytical instrumentation and laboratory methods

- Working knowledge of cGLP / cGMP and applicable FDA, EMA, and ICH regulatory guidelines

- Experience contributing to multidisciplinary scientific teams and cross-functional projects

- Experience mentoring or supervising laboratory personnel preferred

- Strong analytical thinking, scientific judgment, and problem-solving skills

- Excellent written and verbal communication skills

**Why Pharmaron?**

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 21,000 employees and operations in the U.S., the U.K. and China. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

**Collaborative Culture: ** You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

**Benefits:**

As part of our commitment to your well-being, we offer a comprehensive benefits package:

- Insurance including Medical, Dental & Vision with significant employer contributions

- Employer-funded Health Reimbursement Account

- Healthcare & Dependent Care Flexible Spending Accounts

- 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance

- 401k plan with generous employer match

- Access to an Employee Assistance Program

**How to Apply:**

Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!

As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.

**About Pharmaron**

Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China.

Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.

Senior Scientist – Analytical Chemistry

About Genentech

We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.

Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers. 

Our patient resource center is dedicated to getting patients and caregivers to the right resources. You can reach them at 1 (877) GENENTECH (436-3683)
Monday-Friday, 6am-5pm PST or patientinfo@gene.com. 

Community Guidelines:

1. We want to foster positive conversation around the issues we are passionate about. To that end, we remove profanity, content that contains threatening language, content that is aimed at private individuals, personal information, and repeated unwanted messages.

2. Don’t mention any medicines by name — ours or anyone else’s.
Because of the fair balance rules governing our industry, we cannot post any comments that reference any pharmaceutical brand, product, or service. Please do not mention any specific medicines by name, or include any links to third party sites in your comments.

3. This isn’t the place to report or discuss side effects.
This site is not intended as a forum for reporting side effects experienced while taking a Genentech product. Instead, you should report any side effects to Genentech Drug Safety at 1-888-835-2555. You can also report side effects of any prescription product directly to the FDA at 1-800-FDA-1088 or by visiting www.FDA.gov/medwatch.

4. Don’t pitch your product or service.
Please don't use our page as a place to promote your product or pitch your services. Please also avoid posting links to external sites. We reserve the right to remove any posts that are deemed promotional.

Industry: Biotechnology Research
Company Size: 10,001+ employees

Genentech

The Position

We advance science so that we all have more time with the people we love.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Genentech!

**The Opportunity:**

We are seeking a highly motivated Senior Scientist or Principal Scientist with a strong record of laboratory innovation and technical depth to join our Synthetic Molecule Analytical Chemistry (SMAC) group.

This role is ideal for a scientist who thrives at the bench and is excited to solve complex analytical challenges, while contributing to advancing programs spanning discovery through clinical development.

The Scientist will play a key role in advancing a diverse pipeline including synthetic small molecules, peptides, oligonucleotides, and drug delivery systems (e.g., lipid nanoparticles, polymer nanoparticles), working in a highly collaborative, cross-functional environment:

- Designing, developing, and troubleshooting analytical methods from first principles, including sample preparation, method optimization, and data interpretation with state-of-the-art technologies including but not limited to high resolution mass spectrometry (HRMS), UHPLC, 2D-LC/MS, GC/MS, light scattering, spectroscopy, rheology, microscopy.

- Applying and deepen expertise in HRMS, MS/MS, and/or chromatographic separations to solve complex analytical problems during drug discovery/development.

- Contributing to regulatory submissions, including authoring sections and preparing data packages for health authority interactions.

- Partnering with cross-functional teams (process development, formulation, safety science, quality, etc.) to develop control strategies aligned with cGMP, ICH, and regulatory expectations.

- Informing program decisions across discovery and early development, i.e. generating high-quality data to guide molecular and formulation decisions

- Innovating and evaluating new technologies in analytical chemistry or materials characterization to enable the integration of state-of-the-art instrumentation and software to solve complex problems.

- Maintaining a high-level scientific profile both internally and externally in terms of pipeline contributions and scholarly achievements.

**Who You Are**

Successful candidates will possess the following qualifications:

- PhD in Analytical Chemistry, Pharmaceutical Sciences, Materials Sciences, Bioengineering, or relevant scientific disciplines with

0-2 years industry experience ( Senior Scientist); 3-5 years of industry experience (Principal Scientist). Exceptional candidates with Bachelor or Master degree in these fields with 12+ years of experience may be considered. Title and level will be aligned with qualifications and experience.

- Outstanding record of innovation and success in multiple projects over the course of graduate, post-doctoral and industrial career with a sustained publication or patent record.

- Deep hands-on expertise in at least one of the following areas for the analysis of synthetic small molecules, peptides, oligonucleotides, polymers, or nanoparticles (lipid and polymer nanoparticles) is required:

- Mass spectrometry method development (HRMS, MS/MS, structural elucidation)

- Chromatographic method development (reversed phase, normal phase, HILIC, SEC, SFC, 2D-LC/MS)

- Experience with chromatography and/or MS data systems (e.g., Empower, Xcalibur, MassHunter, Chromeleon), and ability to independently analyze complex datasets, is required.

- Experience with nanoparticle-based drug delivery systems (lipid nanoparticles, polymer nanoparticles, etc.) is highly desirable.

- Excellent communication (orally and in writing) and organizational skills.

- Ability to collaborate, learn, and eventually lead in a CMC/cross functional environment.

- Ability to take initiative, think strategically, work in teams and develop people, have advanced literature searching and problem-solving skills.

**Preferred:**

- Knowledge of the chemistry and formulation processes of nanoparticle-based drug delivery systems (e.g., lipid nanoparticles, polymeric systems).

- Exposure to CMC, regulatory submissions, or analytical control strategies.

- Working knowledge of data analysis, modeling, and AI assisted workflows, including the ability to effectively use AI tools (e.g., LLM).

- Familiarity with additional characterization tools (e.g., light scattering, rheology, spectroscopy, microscopy).

Relocation benefits are available for this posting.

The expected salary range for this position based on the primary location of California for Senior Scientist is $124,300- $230,900 and Principal Scientist is $143,200-$265,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

**Benefits**

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Senior/ Principal Scientist, Synthetic Molecule Analytical Chemistry

The Position

We advance science so that we all have more time with the people we love.

A healthier future. It’s what drives us to innovate. To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more time with the people we love. That’s what makes us Genentech!

**The Opportunity:**

We are seeking a highly motivated Senior Scientist or Principal Scientist with a strong record of laboratory innovation and technical depth to join our Synthetic Molecule Analytical Chemistry (SMAC) group.

This role is ideal for a scientist who thrives at the bench and is excited to solve complex analytical challenges, while contributing to advancing programs spanning discovery through clinical development.

The Scientist will play a key role in advancing a diverse pipeline including synthetic small molecules, peptides, oligonucleotides, and drug delivery systems (e.g., lipid nanoparticles, polymer nanoparticles), working in a highly collaborative, cross-functional environment:

- Designing, developing, and troubleshooting analytical methods from first principles, including sample preparation, method optimization, and data interpretation with state-of-the-art technologies including but not limited to high resolution mass spectrometry (HRMS), UHPLC, 2D-LC/MS, GC/MS, light scattering, spectroscopy, rheology, microscopy.

- Applying and deepen expertise in HRMS, MS/MS, and/or chromatographic separations to solve complex analytical problems during drug discovery/development.

- Contributing to regulatory submissions, including authoring sections and preparing data packages for health authority interactions.

- Partnering with cross-functional teams (process development, formulation, safety science, quality, etc.) to develop control strategies aligned with cGMP, ICH, and regulatory expectations.

- Informing program decisions across discovery and early development, i.e. generating high-quality data to guide molecular and formulation decisions

- Innovating and evaluating new technologies in analytical chemistry or materials characterization to enable the integration of state-of-the-art instrumentation and software to solve complex problems.

- Maintaining a high-level scientific profile both internally and externally in terms of pipeline contributions and scholarly achievements.

**Who You Are:**

Successful candidates will possess the following qualifications:

- PhD in Analytical Chemistry, Pharmaceutical Sciences, Materials Sciences, Bioengineering, or relevant scientific disciplines with 0-2 years industry experience ( Senior Scientist); 3-5 years of industry experience (Principal Scientist). Exceptional candidates with Bachelor or Master degree in these fields with 12+ years of experience may be considered. Title and level will be aligned with qualifications and experience.

- Outstanding record of innovation and success in multiple projects over the course of graduate, post-doctoral and industrial career with a sustained publication or patent record.

- Deep hands-on expertise in at least one of the following areas for the analysis of synthetic small molecules, peptides, oligonucleotides, polymers, or nanoparticles (lipid and polymer nanoparticles) is required:

- Mass spectrometry method development (HRMS, MS/MS, structural elucidation)

- Chromatographic method development (reversed phase, normal phase, HILIC, SEC, SFC, 2D-LC/MS)

- Experience with chromatography and/or MS data systems (e.g., Empower, Xcalibur, MassHunter, Chromeleon), and ability to independently analyze complex datasets, is required.

- Excellent communication (orally and in writing) and organizational skills.

- Ability to collaborate, learn, and eventually lead in a CMC/cross functional environment.

- Ability to take initiative, think strategically, work in teams and develop people, have advanced literature searching and problem-solving skills.

**Preferred:**

- Exposure to CMC, regulatory submissions, or analytical control strategies.

- Working knowledge of data analysis, modeling, and AI assisted workflows, including the ability to effectively use AI tools (e.g., LLM).

Relocation benefits are available for this posting.

The expected salary range for this position based on the primary location of California for Senior Scientist is $124,300- $230,900 and Principal Scientist is $143,200-$265,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.

**Benefits**

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants.

Senior/Principal Scientist - Synthetic Molecule Analytical Chemistry, Genentech Research and Early Development

ADM unlocks the power of nature to enrich the quality of life. We’re a premier global human and animal nutrition company, delivering solutions today with an eye to the future. We’re blazing new trails in health and well-being as our scientists develop groundbreaking products to support healthier living. We’re a cutting-edge innovator leading the way to a new future of plant-based consumer and industrial solutions to replace petroleum-based products. We’re an unmatched agricultural supply chain manager and processor, providing food security by connecting local needs with global capabilities. And we’re a leader in sustainability, scaling across entire value chains to help decarbonize our industry and safeguard our planet. From the seed of the idea to the outcome of the solution, we give customers an edge in solving the nutritional and sustainability challenges of today and tomorrow. Learn more at www.adm.com.

Industry: Food and Beverage Manufacturing
Company Size: 10,001+ employees

Analytical Chemistry / Chemometrics Support

This position is located in the ADM R&D Analytical Laboratory, which provides analytical support across ADM’s global portfolio. This role may support both laboratory analyses and applied chemometric and statistical workflows, working closely with senior scientists and cross‑functional teams.

An ideal candidate will have strong hands‑on experience in analytical laboratory techniques, along with familiarity or applied exposure to chemometrics, statistics, or modeling concepts gained through academic coursework or professional experience. This position offers the opportunity to continue developing expertise across a variety of analytical and data analysis techniques through structured technical guidance and mentorship.

**Key Responsibilities**

- Ensure safe work practices are applied for all tasks in the laboratory and throughout ADM facilities.

- Perform routine and non‑routine analytical testing using advanced techniques such as LC/MS, HPLC, GC/MS, GC, ICP, ICP‑MS, FTIR, and laboratory robotics.

- Support the development, optimization, and implementation of analytical methods to meet the needs of ADM business units and customers.

- Assist with chemometric and statistical workflows associated with routine analytical methods and process monitoring, including data preparation, exploratory analysis, model execution, and basic performance evaluation.

- Generate high‑quality laboratory data to support model development, validation, maintenance, and monitoring.

- Contribute to R&D projects requiring analytical data and applied modeling support under the technical direction of senior scientists.

- Collaborate with chemists, engineers, data scientists, and operations partners on cross‑disciplinary projects.

- Communicate results, observations, and potential issues clearly to project stakeholders.

- Perform routine instrument maintenance and basic troubleshooting.

- Prioritize assigned tasks to meet project timelines in a dynamic environment.

- Continue professional development through training, mentoring, and hands‑on experience.

Job Requirements

**Required**

- Bachelor’s or Master’s degree in Chemistry, Biochemistry, Chemical Engineering, Statistics, Data Science, or a closely related field.

- 3–5 years of relevant hands‑on laboratory experience in analytical chemistry or spectroscopy.

- Strong practical experience with analytical laboratory techniques, including chromatographic and/or spectroscopic methods.

- Familiarity with chemometrics, statistics, or modeling concepts.

- Working knowledge of data analysis tools such as JMP, R, Python, Unscrambler, PLS Toolbox, or similar platforms.

- Ability to work independently on defined tasks while contributing effectively within a team environment.

- Strong written and verbal communication skills.

- Understanding of laboratory safety practices and the safe handling of hazardous materials.

**Preferred**

- Experience with food, feed, fermentation, or agricultural matrices.

- Interest in continued growth in chemometrics, spectroscopy, or advanced analytics.

Excited about this role but don’t think you meet every requirement listed? We encourage you to apply anyway. You may be just the right candidate for this role or another one of our openings.

ADM requires the successful completion of a background check.

REF:107220BR

Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours.

If hired, employees will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

The pay range for this position is expected to be between:

$70,400.00 - $129,000.00

**Salaried Incentive Plan**

The total compensation package for this position will also include annual bonus

**Benefits And Perks**

Enriching the quality of life for the world begins by taking care of our colleagues. In addition to competitive pay, we support your diverse needs with a comprehensive total rewards package to enhance your well-being, including:

- Physical wellness – medical/Rx, dental, vision and on-site wellness center access or gym reimbursement (as applicable).

- Financial wellness – flexible spending accounts, health savings account, 401(k) with matching contributions and cash balance plan, discounted employee stock purchasing program, life insurance, disability, workers’ compensation, legal assistance, identity theft protection.

- Mental and social wellness – Employee Assistance Program (EAP), Employee Resource Groups (ERGs) and Colleague Giving Programs (ADM Cares).

**Additional Benefits Include**

- Paid time off including paid holidays.

- Adoption assistance and paid maternity and parental leave.

- Tuition assistance.

- Company-sponsored training and development resources, such as LinkedIn Learning, language training and mentoring programs.

*Benefits may vary for bargained locations, confirm benefit eligibility with your recruiter.

**#IncludingYou**

Diversity, equity, inclusion and belonging are cornerstones of ADM’s efforts to continue innovating, driving growth, and delivering outstanding performance. We are committed to attracting and retaining a diverse workforce and create welcoming, truly inclusive work environments — environments that enable every ADM colleague to feel comfortable on the job, make meaningful contributions to our success, and grow their career. We respect and value the unique backgrounds and experiences that each person can bring to ADM because we know that diversity of perspectives makes us better, together.

We welcome everyone to apply. We are committed to ensuring all qualified applicants receive consideration for employment regardless of race, color, ethnicity, disability, religion, national origin, language, gender, gender identity, gender expression, marital status, sexual orientation, age, protected veteran status, or any other characteristic protected by law

**About ADM**

At ADM, we unlock the power of nature to provide access to nutrition worldwide. With industry-advancing innovations, a complete portfolio of ingredients and solutions to meet any taste, and a commitment to sustainability, we give customers an edge in solving the nutritional challenges of today and tomorrow. We’re a global leader in human and animal nutrition and the world’s premier agricultural origination and processing company. Our breadth, depth, insights, facilities and logistical expertise give us unparalleled capabilities to meet needs for food, beverages, health and wellness, and more. From the seed of the idea to the outcome of the solution, we enrich the quality of life the world over. Learn more at www.adm.com.

**Req/Job ID**

107220BR

Scientist III - Decatur, IL

Welcome to DataAnnotation! We pay smart folks to train AI. We offer a remote, flexible work model- you choose your own hours and get to work when you want, whenever you want. Apply now through our open Job Listings.

Industry: Software Development
Company Size: 5,001-10,000 employees

DataAnnotation

We are looking for a Research Scientist (Chemistry) to join our team to train AI models. You will measure the progress of these AI chatbots, evaluate their logic, and solve problems to improve the quality of each model.

In this role you will need to hold an expert level understanding of chemistry. Other related fields include, but are not limited to: Research and Development Chemist, Formulation Scientist, Development Chemist, Analytical Chemist, Chemical Engineer, Medicinal Chemist, Biochemist, Process Development Chemist.

**Benefits**

- This is a full-time or part-time REMOTE position

- You’ll be able to choose which projects you want to work on

- You can work on your own schedule

- Projects are paid hourly starting at $40+ USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots complex chemistry questions and evaluate their outputs

- Evaluate the quality produced by AI models for correctness and performance

**Qualifications**

- Fluency in English (native or bilingual level)

- Detail-oriented

- Solid knowledge of general, organic, and physical chemistry concepts

- A current, in progress, or completed Masters and/or PhD is preferred but not required

**Notes**

Payment is made via PayPal. We will never ask for any money from you. PayPal will handle any currency conversions from USD. Only applicants in the United States will be considered for this role. This is an independent contract position.

#chem

Research Scientist (Chemistry)

Bell International Laboratories, Inc, is located in Eagan, Minnesota.  We specialize in Health, Beauty and Cosmetic Manufacturing.  Our expertise is in Sun Care, Skin Care, Hair Care,  OTC and Nutritional products.  We offer R&D services as well as product manufacturing.  Bell International Laboratories is fully certified and regulated by the FDA, and is ATF,EPA and Minnesota Department of Health registered.

Industry: Personal Care Product Manufacturing
Company Size: 201-500 employees

Bell International Laboratories

The Analytical Laboratory Chemist is pivotal in conducting and managing analytical testing of raw materials, in-process samples, and finished products to ensure compliance with cGMP standards. This role supports the Quality Control Lab Manager in upholding the integrity and quality of the laboratory environment.

**Responsibilities: **

- Develop and validate analytical methods to ensure reliability and accuracy of test results.

- Operate and maintain sophisticated laboratory instruments, including HPLC, GC, UV-Vis, and FTIR.

- Conduct routine calibration and validation of laboratory instruments to maintain compliance with operational standards.

- Prepare and analyze samples from raw materials, in-process batches, and finished products using both wet chemistry techniques and instrumental analysis.

- Maintain meticulous laboratory records and notebooks, ensuring detailed documentation following regulatory requirements.

- Collaborate with team members to efficiently complete testing assignments within set timelines.

- Monitor ongoing product quality to confirm adherence to established standards and specifications.

- Adhere to Standard Operating Procedures (SOPs) and global methodological standards such as USP, AOCS, and ASTM.

- Troubleshoot and perform minor repairs on analytical instruments to minimize downtime.

- Implement safety protocols for handling chemicals, managing laboratory waste, and maintaining a clean lab environment.

- Organize and manage laboratory inventory to ensure availability of necessary supplies and equipment.

- Mentor and train new laboratory personnel on testing procedures and instrument operations.

**Required Skills/Abilities: **

- Proficient in the use of standard laboratory equipment and familiar with advanced analytical techniques.

- Excellent communication skills, both verbal and written, with the ability to convey complex information clearly.

- Strong analytical thinking and problem-solving capabilities.

- Effective time management skills to handle multiple tasks and meet strict deadlines.

- Demonstrated ability to work autonomously in a dynamic, fast-paced environment.

- Keen attention to detail with a commitment to high-quality work.

- Flexibility to adapt to new procedures or rapid changes in project priorities.

- Proficient in Microsoft Office

**Required Education and Experience: **

- Bachelor’s degree in Chemistry, Biochemistry, or a related scientific field.

- 3 to 5 years of hands-on experience in an analytical laboratory setting, preferably within the personal care, pharmaceutical, or related industries.

- Extensive knowledge of cGMP practices, organic chemistry, and instrumental analytics (HPLC, GC, UV-Vis, FTIR).

Analytical Chemist

Pay Rate Low: 40 | Pay Rate High: 45

Seeking a Chemist to join a world leader in science. Opportunity to join an R&D Analytical Characterization team, supporting chromatography and wet chemistry testing of materials used in medical/surgical products. This role focuses on analyzing small organic compounds, additives, degradation products, and impurities in complex polymer systems.

Key Responsibilities

- Perform analytical testing using GC, Headspace GC, and U/HPLC-UV.

- Conduct full workflows including sample preparation, method execution/qualification, data analysis, and reporting.

- Investigate and report issues such as OOS/OOT results, instrument problems, and lab deviations.

- Troubleshoot and maintain analytical instruments.

- Document work in compliance with FDA/ICH standards and internal procedures.

- Communicate results clearly through written reports and presentations.

- Support preparation of technical reports and documentation

**Qualifications**

- BS, MS, or PhD in Chemistry (Analytical, Polymer, Organic) or related field

- ~1–2+ years of relevant experience (depending on degree level)

- Familiarity with medical device or regulated environments preferred

- Strong foundation in analytical chemistry principles

- Hands-on experience with GC and HPLC instrumentation

- Experience with method development/validation (preferred)

Belcan, a Cognizant company is a global supplier of engineering, manufacturing & supply chain, workforce and government IT solutions to customers in the aerospace, defense, commercial vehicles & automotive, industrial, and private sector. We engineer better outcomes for our customers – from jet engines, airframe, and avionics to heavy vehicles, automobiles, and cybersecurity. 

Taking a partnering approach to provide solutions that are adaptable, integrated, and value added, we have been earning the trust of our customers for over 60 years and counting.

Industry: Information Technology & Services
Company Size: 5,001-10,000 employees

Belcan

Job Title: Research Associate I

Location: Wilmington, DE

Zip Code: 19803

Pay Rate: $30-33/hr

Keyword's: #Wilmingtonjobs; #Associatejobs.

Start Date: Immediate

Job Description:

Responsibilities:* Lead application focused research efforts that provide direct technical support to R&D projects in paints and coatings, construction materials, water, and the energy industries, fostering innovation.

* Contribute to the development of novel formulations using new and existing active ingredients and next-generation delivery technologies.

* Utilize analytical chemistry techniques, including HPLC, to characterize the performance criteria of new formulations.

* Collaborate with lead scientists, other research associates, and broader interdisciplinary teams, including regulatory, marketing, and product development, to support and drive projects from concept to commercialization.

* Effectively manage time across multiple projects and competing demands, demonstrating a proactive approach to execution.

* Maintain a safe and organized laboratory environment while assuring compliance with safety regulations.

Qualifications:* Bachelors or Masters degree in Chemistry, Biochemistry, or Chemical Engineering.

* A minimum of 3 years of industrial laboratory experience in a research, product development, or technical application setting.

* Prior experience with analytical techniques (HPLC) and industrial product formulation a plus.

* Strong written and verbal communication skills, with the ability to collaborate across teams.

* Self-motivated with the ability to manage multiple projects and shifting priorities in a fast-paced environment.

* Strong problem-solving skills and creative thinking.

* Experience working in a team-oriented research setting to drive projects toward completion preferred.

Associate Researcher

ARL Bio Pharma is a contract laboratory that provides analytical and microbiological testing for the pharmaceutical industry. Since 1998, ARL has supported the industry-wide commitment to deliver high-quality drug products by providing guidance and test services for all phases of the product lifecycle following USP, FDA, and ICH guidelines.

Whether you are a raw material supplier, equipment manufacturer, pharmaceutical manufacturer, pharmacy, or health-system we provide the testing needed to get your drug products ready for release.

ARL’s dedicated team oversees the entire process from understanding your goals to providing results and helping interpret the data.

ARL Bio Pharma is an FDA registered and audited analytical laboratory and DEA licensed for Schedules I through V. The laboratory is ISO 17025:2017 accredited as applicable to our scope of accreditation. 17025:2017 accreditation independently demonstrates ARL's ability to not only comply with quality requirements, but to competently perform specified tests and activities.

Industry: Pharmaceutical Manufacturing
Company Size: 201-500 employees

ARL Bio Pharma

Chemist I - Analytical

Position Summary

Join a company where you can make a difference from day one and help make the world a better and safer place. ARL Bio Pharma provides analytical and microbiological testing for the pharmaceutical industry. Our laboratory works with pharmaceutical companies, compounding and hospital pharmacies, drug manufacturers, and raw material suppliers bringing excellence to pharmaceutical sciences and making pharmaceuticals safer.  This position is a fantastic stepping-stone for those with some basic experience looking to expand their career in the interesting world of the pharmaceutical industry.  The Chemist I is responsible for utilizing established methods and standard lab equipment/instrumentation (HPLC, IC) to qualitatively and quantitatively analyze routine pharmaceutical substances and formulations.

**Some highlights... **

- Paid Training

- Work in a comfortable office setting with casual dress code

- Have your own workspace where you can work largely independently

- Free Medical and Dental insurance

- 401K Retirement with Company Match

- Excellent Work/Life Balance

This is a full-time role with a great benefits package.

**Work Schedule: ** 7:00 am - 4:30pm

**Restrictions: **  Because of vital nature of this work, we do not allow medical marijuana cards and we do random drug testing on all of our employees.

**Essential Functions **

- Adhere to Quality Management System (QMS)

- Follow prescribed safety rules and regulations in performing all assigned duties

- Follow written and oral instruction

- Prepare reagents and solutions required for testing

- Perform laboratory testing and record results in compliance with cGMP’s (if applicable) and internal QMS

- Work and think independently, yet share ideas and work towards team goals

- Use a personal computer including word processing, spreadsheets, email and database applications

- Express thoughts in a clear concise manner both orally and written

- Work to establish the ability to effectively prioritize and plan multiple work activities with varying deadlines and complexities

- Adherence to all ARL safety standards, protocols, policies and procedures

**Position Requirements... **

- An associate degree in chemistry or related science with 2+ years industrial experience OR...

- Bachelor’s degree in chemistry or related science with 1-2 years’ experience in the Pharmaceutical industry.

- Communication Proficiency

- Problem Solving/Analysis

- Organization/Multi-tasking

- Collaboration Skills

- Thoroughness

**Work Environment... **

This job operates in a laboratory environment.

**Physical Demands... **

The role requires standing for prolonged periods of time; dexterity in fingers and hands to perform complex and precise manipulations; ability to walk and stoop; ability to lift and move up to 50 pounds; see in the normal visual range including the ability to distinguish colors and shades and hear in the normal audio range with or without correction.

AAP/EEO Statement

ARL Bio Pharma, Inc.  provides equal employment opportunity to all individuals regardless of their race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  ARL Bio Pharma, Inc. expressly prohibits any form of workplace harassment based on race, color, creed, religion, gender, age, sexual orientation, gender identity, national origin, disability, veteran status, genetics or any other characteristic protected by state, federal, or local law.  Improper interference with the ability of ARL Bio Pharma, Inc.  employees to perform their job duties may result in discipline up to and including discharge. Further, the company takes affirmative action to ensure that applicants and employees are treated without regard to any of these characteristics.

Since the beginning, ZRT has maintained a singular focus: helping people get and stay healthy.

With 20 years of experience and results from over 8 million tests, ZRT Laboratory is a recognized leader in innovative and meaningful hormone, neurotransmitter and elements testing. 

Individuals, health care providers in all 50 states and 90 countries, and research teams worldwide use our tests, including the CDC, the NIH and many renowned universities.

ZRT is the recognized leader in saliva and dried blood spot testing for hormones, and holds the distinction of being the lab that developed dried urine testing for hormones.

ZRT was founded and is led by David Zava, PhD, a renown expert in hormones and breast cancer. He is an author, researcher and frequent lecturer at industry events.

Learn more about the role of hormones, neurotransmitters and elements in our health at https://www.zrtlab.com/blog/.

Industry: Hospitals and Health Care
Company Size: 51-200 employees

ZRT Laboratory

ZRT Laboratory is an internationally recognized leader in hormone and wellness testing. For over 27 years, healthcare providers and academic research teams worldwide have trusted our expertise in accurately measuring hormones, neurotransmitters, and elements in saliva, finger-stick dried blood, dried urine, and serum. With results from over 10 million tests, ZRT offers a commitment to the best science and the best people, delivering premier personalized home-collection testing solutions.

**Position Summary: **

As an Analytical Chemist at ZRT Laboratory, you will play a hands-on role in the development and execution of LCMS and GCMS methodologies, contributing directly to the accuracy and advancement of our hormone and wellness testing. Working in our CLIA-certified high complexity laboratory, you will analyze complex biological samples, support method development, and help ensure the quality and integrity of results that matter to patients and providers worldwide.

**Key Responsibilities: **

~~Production & Analysis: ~~

- Perform commercial, clinical, and research sample preparation, analysis, and documentation

- Create and maintain assay standards, calibrators, and controls

- Rotate between laboratory areas as needed

~~Instrumentation & Laboratory Operations: ~~

- Operate and maintain a wide range of instrumentation

- Prepare reagents, manage inventory, and perform equipment maintenance

- Handle biohazard waste disposal

~~Data Management & Documentation: ~~

- Ensure accuracy of data and maintain records

- Document and communicate ongoing and completed projects promptly

~~Quality & compliance: ~~

- Maintain competency in assigned testing procedure

- Ensure compliance with SOPs and state and federal regulations

- Maintain HIPAA compliance

- Adhere to proper hand hygiene and PPE protocols

~~Professional Development & Administrative Support: ~~

- Participate in continuing education programs

- Support ordering and budgeting activities

**Competencies: **

- Strong problem-solving skills to troubleshoot LCMS/GCMS issues and optimize methods

- Strong written and verbal communication skills for clear reporting and presentation of analytical results

- Detail-oriented with a strong commitment to maintaining high data quality and laboratory standards

- Ability to work both independently and collaboratively within a team

Required Education and Experience:

- Master's degree or higher in Analytical Chemistry or a related field

- Five years of prior LC/GC-MS experience including instrument operation and data analysis

ZRT Laboratory is an equal opportunity employer. We are committed to building a diverse and inclusive workplace where all employees feel valued and supported.

Job Type: Full-time

Benefits:

- 401(k)

- 401(k) matching

- Dental insurance

- Employee assistance program

- Employee discount

- Flexible schedule

- Flexible spending account

- Health insurance

- Life insurance

- Paid time off

- Parental leave

- Referral program

- Tuition reimbursement

- Vision insurance

Analytical Chemist - LCMS

**Job Title**

Scientist II, Analytical Chemistry

**Job Description**

**The Role:**

Our site in **Burnet, TX **is seeking a **Scientist II, Production Analytical Chemist, ** to join our team. Come help analyze and characterize the materials that help design, deliver, and optimize some of the most critical semiconductor devices in the world. Be a part of a team and organization that is pushing the boundaries of chemical manufacturing through your expertise as an analytical chemist!

We are seeking a Chemist with in-depth knowledge of analytical chemistry and techniques applied to the characterization of complex mixtures. This knowledge is required to troubleshoot, develop, and optimize analytical methods for routine and non-routine QC analysis to support the Manufacturing and Engineering Teams. Due to the complex nature of sample matrices, this opportunity allows the right person to expand upon their technical skill set and participate on a dynamic team in a growing organization.

The ideal candidate will be results and detail oriented, strive to be an excellent team player, and be able to apply their solid knowledge of chemistry, mechanical inclination, good lab practices, and familiarity with the criticality of materials science in the semiconductor industry.

**What You'll Do**

- Demonstrate leadership in maintaining safety and quality culture

- Prepare and conduct chemical and/or physical analyses as defined by existing work instructions on routine and non-routine samples using analytical instruments including: ICP-MS, ICP-OES, GC, GC/MS, HPLC, IC, XRF, UV-Vis, NIR, KF, etc.

- Document, process, transfer, and review analytical data to ensure completion, conformity, traceability, and validity and support production and other internal/external customer needs; Take corrective action when necessary

- Maintain instrumentation, tools, chemicals, and consumables required for product testing purposes

- Effectively troubleshoot instruments and resolve any hardware or software issues

- Verify the efficacy of samples and ensure that all samples and chemicals are properly stored or disposed

- Propose/Lead/Support initiatives to foster continuous improvement of new or existing testing methods and practices

- Maintain housekeeping and proper Laboratory cleanliness to support high quality trace-level data

- Compile and present data and presentations to communicate data and other relevant information for continuous improvement, method development/validation, and other projects

- Work on cross-functional teams as the analytical subject matter expert

- Train other personnel to analyze samples or perform other laboratory tasks

**What We Seek**

- A minimum of a Bachelor's Degree in Analytical Chemistry or relevant area of study is required.

- 2+ years of experience in operating, troubleshooting, and maintaining analytical instrumentation (LC, LC-MS, IC, IC-MS, GC, GC-MS, ICP-MS, ICP-OES), ICP-MS, trace metals, and cleanroom experience strongly preferred

- Advanced computer knowledge, including MS Office; LIMS experience preferred

- Knowledge and demonstration of proper safe handling/disposal of chemicals and ability to maintain a clean and safe workspace

- Proven record of completing lab work safely, correctly, efficiently, timely, and independently

- Expand upon personal job knowledge by participating in educational opportunities, special project teams, and reading technical publications

- Ability to multi-task and balance independent, teamwork, and time effectively

- Dedication to meticulous attention to detail and organization

- Strong dexterity, good eye-hand coordination, and ability to safely perform routine repetitive motions

- Advanced mechanical inclination and experience operating electrical and nonelectrical laboratory equipment

- We are looking for a first shift Mon-Fri, Weekends/Holidays as needed

**Why Work at Entegris**

Lead. Inspire. Innovate. Define Your Future.

Not everyone who works for a global company shares the same background, experiences and perspectives. We leverage the differences of our employees to bring new ideas to the table. Every employee throughout the company is encouraged to share input on projects and initiatives. Our decision-making process is truly a collaborative effort as we realize there are leaders at every level of the organization. We put our values at the core of how we operate as an organization - not just when it's convenient, but in a lasting and meaningful way. We want the time and energy you spend here to have a positive impact on your life inside and outside of the office

**What We Offer**

Our total rewards package goes above and beyond just a paycheck. Whether you're looking to build your career, improve your health, or protect your wealth, we offer generous benefits to help you achieve your goals.

- Generous 401(K) plan with an impressive employer match

- Excellent health, dental and vision insurance packages to fit your needs

- Flexible work schedule and 11 paid holidays a year

- Paid time off (PTO) policy that empowers you to take the time you need to recharge

- Education assistance to support your learning journey

- Values-driven culture with colleagues that rally around People, Accountability, Creativity and Excellence

Entegris does not provide immigration-related sponsorship for this role. Do not apply for this role if you will need Entegris immigration sponsorship (e.g., H1B, TN, STEM OPT, etc.) now or in the future.

At Entegris we are committed to providing equal opportunity to all employees and applicants. Our policy is to recruit, hire, train, and reward employees for their individual abilities, achievements, and experience without regard to race, color, religion, sexual orientation, age, national origin, disability, marital or military status.

Scientist II, Analytical Chemistry

TALENT Software Services is a Service Disabled Veteran-Owned Small Business (SDVOSB) providing the best IT Consulting and Professional Services nationwide for over 35 years. We are one of the most trusted partners for delivery of Project, Data Management, Application, and Infrastructure Services,  TALENT staffs technologies including Java, .NET, Project Management, Analytics, Architecture, and more. 

Representation that counts:  This is where top Twin Cities TALENT find their value in the local marketplace.

"It's easy to get the job done when you're surrounded by TALENT! "

Industry: IT Services and IT Consulting
Company Size: 51-200 employees

TALENT Software Services

**Qualifications**

-  BA/BS (6 yrs.) of relevant experience in analytical chemistry or biologics testing lab

-  MS (4 yrs.) of relevant experience in analytical chemistry or biologics testing lab

-  Ph.D. (1-2 yrs.) of relevant experience in analytical chemistry or biologics testing lab

**Required Skills And Experience**

-  Must have separations experience for large molecules or plate-based assay experience.

-  Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using at least one of the following techniques:

- Liquid Chromatography (HPLC / UPLC)

- Protein A Titer, Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX, AEX, CEX), Reverse Phase (RP), or Hydrophobic interaction chromatography (HIC)

- Electrophoretic methods such as capillary electrophoresis sodium dodecyl sulfate (CE-SDS) and/or capillary isoelectric focusing (cIEF)

-  Basic instrumentation troubleshooting

-  Ability and willingness to train and follow laboratory methods and procedures

-  Familiarity with Microsoft Office Applications (Outlook, Excel, Word, PowerPoint, OneNote, Teams, etc.)

-  Making accurate reagent preparations (dilutions / solutions / buffers / mobile phases)

-  Good documentation practices & utilization in electronic lab notebooks (ELN)

**Desired Skills And Experience**

-  Analytical software such as Empower.

-  Experience in analyzing biologics including monoclonal antibodies and/or other therapeutic proteins using plate-based methods, e.g., ELISA (HCP, proA)

-  Familiarity with compendial testing such as UV 280, pH, and Physical Observations

Notes:

-  Open to bachelor, masters, and/or PhD level.

-  100% onsite lab based role.

-  Required to have direct expertise in operating LC and CE analytical systems for testing large molecules in an industry or CRO environment.

-  Required to be experienced in the industry, with ability to quickly train on ***-specific procedures and start working in the lab.

-  Role will involve high volume sample testing across multiple preclinical and clinical stage biologics programs, including proteins and antibody-drug conjugates.

-  Required to follow all safety, compliance and quality practices.

-  Required to understand and follow good documentation practices within an electronic laboratory notebook.

-  Required to have strong communication skills, ability to collaborate, and ability to work independently.

**Description**

Support of routine Biologics analytical testing of samples from cell-line development, in-process, process development/characterization, forced degradation, release & stability, and pre-formulation.

**Responsibilities**

-  Support of high-throughput, pre-formulation, pre-qualification, robustness, or admixture testing

-  Results processing and documentation by following appropriate methods / protocols / procedures

-  Sample management and monitoring of controlled temperature units.

-  Following all appropriate laboratory safety and hygiene procedures.

Scientist - II (Associate)

When progress demands experience, that’s where we come in. 

Yoh is in the business of moving things forward: projects, people, and possibility, delivering the expertise, methodology, and momentum that keep work moving.

From consulting and staffing to enterprise workforce solutions, we bring the expertise to move your business ahead, today and for decades to come. Everything’s aligned and integrated to client needs. 

If it’s powered by science, built by engineers, or driven by data, Yoh is there, embedded in the workforce solutions that move industries ahead. We partner with innovators and problem-solvers who are transforming the marketplace from the inside out. By combining domain expertise with delivery discipline, we turn complex ideas into measurable outcomes.

Nearly a century after our founding, Yoh remains STEM-centered, values-charged, and fully focused on improving business operations and outcomes. Yoh works wherever progress moves fast, with: industries defined by innovation, compliance, and transformation. Our flexible, scalable approach helps the world's best and brightest companies deliver impact. Yoh is a proud member of the Day & Zimmermann family of companies.

Industry: Staffing and Recruiting
Company Size: 1,001-5,000 employees

Yoh, A Day & Zimmermann Company

**Analytical Chemist**

**St. Louis, MO or Durham, NC - ONSITE**

**1 Year W2 contract (with potential to extend or transition to perm)**

**Pay rate: $35-43/hr - Depending on Education and Experience**

**MUST HAVE QUANTITATIVE METHOD DEVELOPMENT WITH LC-MS/MS**

**Shift: **First Shift

**Summary: **

- Participate and assist in planning and conducting activities to develop new products or methods/techniques within the Clinical Microbiology product portfolio in full compliance with current quality and safety standards

- Provide technical assistance for activities to improve or support existing products, methods or techniques.

**Responsibilities: **

- Perform routine analytical testing & develop analytical methods based on the product development & support needs by using effective and efficient design control techniques.

- Participates in the execution of validation protocols.

- Operate, maintain, and troubleshoot lab equipment including: Sciex LC-MS/MS, Agilent HPLC-UV-ELSD, Thermo IC.

- Responsible for an accurate data analysis process. Plans, evaluates, solves issues, collects data and as well as contributes to the interpretation of results together with team, and deduces further work to be carried out. Prioritizes activities to meet deadlines

- Provide technical input and design standard experiments to optimize experimental performance or investigate failure mode to support operations for existing products, methods, or techniques.

- Creates and presents reports on conducted experiments.

- Performs scientific publications watch and stays informed of the latest advances of a specific expertise area. Contributes to scientific publications.

- Contributes to continuous improvement initiatives.

- Follow company health & safety policies for using chemicals and disposal of chemical waste.

**Skills or Requirements: **

- Bachelors Degree

- Method development with LC-MS and MS REQUIRED

- Proficient in Microsoft Word & Excel required

- Knowledge of cGMP and FDA regulations.

- Good oral and written communications skills in English

- Ability to effectively organize, multitask, and work in a fast-paced, deadline driven work environment with attention to detail

- Achievement oriented individual possessing intellectual curiosity

- Flexible with ability to work independently to achieve goals while working apart from direct supervision

**What’s In It For You?**

We welcome you to be a part of one of the largest global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you.

- Medical, Dental & Vision Benefits

- 401K Retirement Saving Plan

- Life & Disability Insurance

- Direct Deposit & weekly ePayroll

- Employee Discount Programs

- Referral Bonus Programs

**Estimated Min Rate **: $29.40

**Estimated Max Rate **: $42.00

**What’s In It for You?**

We welcome you to be a part of the largest and legendary global staffing companies to meet your career aspirations. Yoh’s network of client companies has been employing professionals like you for over 65 years in the U.S., UK and Canada. Join Yoh’s extensive talent community that will provide you with access to Yoh’s vast network of opportunities and gain access to this exclusive opportunity available to you. Benefit eligibility is in accordance with applicable laws and client requirements. Benefits include:

- Medical, Prescription, Dental & Vision Benefits (for employees working 20+ hours per week)

- Health Savings Account (HSA) (for employees working 20+ hours per week)

- Life & Disability Insurance (for employees working 20+ hours per week)

- MetLife Voluntary Benefits

- Employee Assistance Program (EAP)

- 401K Retirement Savings Plan

- Direct Deposit & weekly epayroll

- Referral Bonus Programs

- Certification and training opportunities

Note: Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description. All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit **https://www.yoh.com/applicants-with-disabilities ** to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act. All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

By applying and submitting your resume, you authorize Yoh to review and reformat your resume to meet Yoh’s hiring clients’ preferences. To learn more about Yoh’s privacy practices, please see our Candidate Privacy Notice: **https://www.yoh.com/privacy-notice **

**Job Description**

Join our Discovery Pharmaceutical Science (DPS) team in West Point, PA and play a central role in shaping the next generation of drug candidates. DPS is a cross-functional research organization that delivers drug delivery, solid-state science, pharmaceutical chemistry, and formulation expertise to accelerate Drug Discovery and early Drug Product Development. As a Senior Scientist on our team, you will directly influence the physicochemical design and formulation strategies of preclinical drug candidates across multiple modalities.

**What You’ll Do**

- Lead physicochemical characterization of potential preclinical candidates, using those insights to guide design and formulation decisions.

- Identify and develop fit-for-purpose oral and parenteral formulation strategies for preclinical and clinical studies.

- Plan and execute R&D studies across a variety of administration routes and modalities, including small molecules, peptides, biologics, and vaccines.

- Generate, analyze, and present high-quality data that informs go/no-go decisions for candidate progression to clinical assessment.

- Perform studies such as solubility and crystalline-phase analysis, physical and chemical stability testing (including biologics and vaccines), and in vitro evaluation of modified-release dosage forms, as relevant to modality and delivery route.

- Collaborate closely with cross-functional partners—including Safety Assessment, Process Research, Analytical Chemistry, and DMPK—to support selection and advancement of clinical candidates.

- Act as an embedded scientific contributor on multidisciplinary discovery teams within infectious disease and neuroscience, helping translate pharmaceutical science principles into actionable program decisions.

~~Your work will directly impact which molecules advance toward clinical testing and how they are formulated for safety, stability, and patient delivery. You’ll join a dynamic team where scientific insight, creativity, and collaboration accelerate real-world drug development.~~

**Educational Requirements**

- Postdoctoral training or Ph.D. in Chemistry or related field: or

- M.S. in one of the above fields plus at least 3 years of industry experience: or

- B.S in one of the above fields plus at least 5 years of industry experience

**Experience & Skills**

- Excellent verbal and written communication skills are required.

- Strong leadership/interpersonal skills.

- Motivation to work in a team environment with cross functional interactions are essential.

eligibleforERP

PSCS

**Required Skills**

Accountability, Accountability, Adaptability, Analytical Chemistry, Bioprocessing, Clinical Evaluations, Cross-Functional Collaboration, Cross-Functional Teamwork, Data Analysis, Deep Learning, Drug Delivery, Drug Delivery Technology, Drug Development, Flow Cytometry, High-Throughput Screening, Immunotherapy, Innovative Thinking, Interpersonal Relationships, In Vitro Assays, In Vitro Studies, Medicinal Chemistry, Molecular Biology Techniques, Multi-Color Flow Cytometry, Preformulation, Process Optimization {+ 4 more}

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

**Requirements**

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

**San Francisco Residents Only: ** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

**Los Angeles Residents Only: ** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

**Search Firm Representatives Please Read Carefully**

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

n/a

**Job Posting End Date**

05/6/2026

- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

**Requisition ID: **R389722

Senior Scientist - Discovery Pharmaceutical Sciences

Work Location: Billerica, Massachusetts

Shift: No

Department: HC-RD-XO4 Oligonucleotide Chemical Conjugation

Recruiter: Beverly Dellisola

**This information is for internals only. Please do not share outside of the organization.**

**Your Role**

EMD Serono in Billerica, MA is seeking a Senior Scientist - Oligo Bioinformatics to add to their Oligonucleotide Therapeutics Group (DDTech).

**Responsibilities**

- Develop pipelines that determine mapping coordinates and homology of oligonucleotides to genomes and transcriptomes

- Design and build pipelines that process and analyze related data, store summary results and integrate with the corporate ELN

- Develop pipelines that determine mapping coordinates and homology of oligonucleotides to genomes and transcriptomes

- Develop, deploy, manage, and run applications using Docker containers

- Discovery and development of oligonucleotide therapeutics

**Who You Are**

**Minimum Qualifications:**

- PhD in Chemistry, Chemical Engineering, Computer Science or other Science field with 3+ years of direct experience in siRNA/ASO/SSO

**Preferred Qualifications**

- Experience with common human genetics resources and techniques

- Deployment of interactive applications from scripting languages like R and Python (Shiny and streamlit)

- Experience with relational databases; hands on experience with MySQL

- Experience in common NGS analyses task such mapping reads, quantification of gene expression, and/or variant calling

- Experience with common bioinformatics tools like Samtools, GATK, Bowtie, HISAT2, BLAST, htseq-count, DESeq, Salmon, STAR, or Subread

- Knowledge of Illumina sequencing data analysis is necessary and experience with PacBio and/or Nanopore sequencing

- Familiarity with UNIX computing environment and proficiency in either Python or R scripting

- Experience with docker and Nextflow pipeline

- Ability to communicate finding of NGS data to a general scientific audience in both oral and written forms

Pay Range for this position: $111,100 - $166,600

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click **here**

The Company is an Equal Employment Opportunity employer. No employee or applicant for employment will be discriminated against on the basis of race, color, religion, age, sex, sexual orientation, national origin, ancestry, disability, military or veteran status, genetic information, gender identity, transgender status, marital status, or any other classification protected by applicable federal, state, or local law. This policy of Equal Employment Opportunity applies to all policies and programs relating to recruitment and hiring, promotion, compensation, benefits, discipline, termination, and all other terms and conditions of employment. Any applicant or employee who believes they have been discriminated against by the Company or anyone acting on behalf of the Company must report any concerns to their Human Resources Business Partner, Legal, or Compliance immediately. The Company will not retaliate against any individual because they made a good faith report of discrimination.

Senior Scientist - Oligo Bioinformatics

**Job Description**

The Materials and Biophysical Characterization group in Analytical Research and Development is seeking a highly self-motivated and innovative scientist with deep knowledge and strong problem-solving skills in biophysical characterization. The Biophysical Characterization team is responsible for building the mechanistic understanding of the interplay between formulation composition, process and stability of drug substance and drug product to ensure process robustness and product quality.

As a Senior Scientist, you will be supporting projects in the diverse pipeline by developing and implementing biophysical and particle characterization assays collaborating with process, formulation and device as part of the CMC development team. You are expected to use your scientific expertise to find creative solutions to challenging problems which require deep analytical insight and critical thinking. Additional responsibilities include authoring technical reports and regulatory documents, presenting technical data, and project management. You will conduct independent research, publish research findings, present at scientific conferences, and engage with various external scientific societies/organizations. This is an excellent growth and learning opportunity to work in an exciting, collaborative environment with a wide array of scientists from different divisions and make significant contributions towards our life-saving medicines.

**Education Minimum Requirement**

- Ph.D. in Biophysics, Biochemistry, Chemistry, Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline with 0-4 years’ experience; OR

- MSc in Biophysics, Biochemistry, Chemistry, Chemical Engineering, Biomedical Engineering, Pharmaceutical Sciences or related discipline with 4-8 years’ experience.

**Required Experience And Skills**

- Fundamental understanding of protein science, protein stability, and protein-protein interactions

- Hands-on experience with biophysical and particle characterization techniques for biotherapeutics characterization, excellent analytical skills and the ability to analyze and interpret complex data sets

- Self-motivated with an outstanding scientific track-record; Track-record of independent problem-solving applying deep technical and subject matter expertise

- Excellent interpersonal and communication skills, actively engages in two-way communication to build trusting relationships.

- Excellent organizational skills to multi-task and manage multiple projects.

- Ability to drive operational excellence by clarifying and translating priorities into actionable steps, and ensure expectations are met aligned with agreed standards and methodologies

**Desired Experience And Skills**

- Experience with molecular modeling.

- Experience with cryoEM, BioNMR and/or Mass Spectrometry.

- Experience with biological formulation development and analytical method development.

- Experience with various modalities including peptides, mAbs, ADC, fusion proteins

#AR&D

**Required Skills**

Accountability, Adaptability, Bioprocessing, Cross-Functional Teamwork, Data Analysis, Drug Delivery Technology, Flow Cytometry, High-Throughput Screening, Innovative Thinking, Interpersonal Relationships, Molecular Biology Techniques, Multi-Color Flow Cytometry, Parasitology, Preformulation, Process Optimization, Protein Biochemistry, Protein Purifications, Scientific Research

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

**Requirements**

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

**San Francisco Residents Only: ** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

**Los Angeles Residents Only: ** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

**Search Firm Representatives Please Read Carefully**

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

No

**Travel Requirements**

10%

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

N/A

**Job Posting End Date**

04/30/2026

- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

**Requisition ID: **R387170

Sr. Scientist, Preclinical Dev.

Los Alamos National Laboratory is one of the world’s most innovative multidisciplinary research institutions. We're engaged in strategic science on behalf of national security to ensure the safety and reliability of the U.S. nuclear stockpile. Our workforce specializes in a wide range of progressive science, technology and engineering across many exciting fields, including space exploration, geophysics, renewable energy, supercomputing, medicine and nanotechnology.

Industry: Research Services
Company Size: 10,001+ employees

Los Alamos National Laboratory

**What You Will Do**

Successful candidates will engage in a combination of instrumentation development and original scientific research, tailored to their background and interests. Specific activities may include:

- Supporting the development, calibration, testing, and operation of space plasma instrumentation, including instruments for NASA's IMAP mission and current national security-related space systems

- Contributing to the design and development of instrumentation for future space missions

- Performing original research in one or more of the following areas:

- Heliospheric physics

- Magnetospheric or ionospheric physics

- Solar wind-plasma interactions

- Energetic neutral atom (ENA) measurements

- Analyzing and interpreting space-based data, and disseminating results through peer-reviewed publications and conference presentations

- Postdoctoral researchers are encouraged to develop an independent scientific identity while collaborating closely with senior scientists, engineers, and other postdocs across observational, computational, and theoretical efforts.

**What You NeedMinimum Job Requirements:**

- Ph.D. completed within the past five years (or soon to be completed) in Space Physics, Physics, Astronomy, Engineering, or a closely related field

- Demonstrated research experience relevant to space plasma physics or space instrumentation

- Ability to obtain a DOE Q clearance, which typically requires U.S. citizenship

**Education/Experience**

By the start of the position the applicant must have completed a Ph.D. in a relevant STEM field.

**Desired Qualifications:**

- Laboratory experience relevant to space plasma or ENA instrumentation (e.g., detectors, electronics, calibration facilities, vacuum systems)

- Familiarity with, or strong interest in learning about, heliophysics and space plasma environments (e.g., magnetospheres, solar wind, heliosphere)

- Experience with data analysis, modeling, or simulation related to space-based measurements

- Strong communication skills and interest in collaborative, interdisciplinary research

**Work Location: ** The work location for this position is onsite and located in Los Alamos, NM. All work locations are at the discretion of management.

**Salary: ** Competitive salaries are based on the date the PhD degree requirements were completed or the degree was awarded. Starting salary for a new graduate is currently $97,000. For more information go to Postdoc Program website at https://www.lanl.gov/careers/career-options/postdoctoral-research/index.php .

**Note to Applicants:**

-  For full consideration, please submit (A) a cover letter describing background and relevant experience, (B) a full CV/resume, and (C) contact information for three professional references.

- This appointment is valid for two years with a possible third year extension.

-  Minimum starting salary for a postdoctoral researcher is $97,000 and can increase with post-PhD experience and fellowships.

- US citizenship is not a requirement

- Review of applications will begin as soon as applications are received and until the position is filled

- Strong candidates may be eligible for a Laboratory fellowship. See https://www.lanl.gov/careers/career-options/postdoctoral-research/postdoc-program/postdoc-appointment-types.php  for details.

- For additional information, please contact Carlos Maldonado (cmaldonado@lanl.gov ) or Ruth Skoug (rskoug@lanl.gov).

**Note to Applicants:**

Due to federal restrictions contained in the current National Defense Authorization Act, citizens of the People's Republic of China-including the special administrative regions of Hong Kong and Macau-as well as citizens of the Islamic Republic of Iran, the Democratic People's Republic of Korea (North Korea), and the Russian Federation, who are not Lawful Permanent Residents ("green card" holders) are prohibited from accessing facilities that support the mission, functions, and operations of national security laboratories and nuclear weapons production facilities, which includes Los Alamos National Laboratory.

**Where You Will Work**

Located in beautiful northern New Mexico, Los Alamos National Laboratory (LANL) is a multidisciplinary research institution engaged in strategic science on behalf of national security. Our generous benefits package includes:

- PPO or High Deductible medical insurance with the same large nationwide network

- Dental and vision insurance

- Free basic life and disability insurance

- Paid childbirth and parental leave

- Award-winning 401(k) (6% matching plus 3.5% annually)

- Learning opportunities and tuition assistance

- Flexible schedules and time off (PTO and holidays)

- Onsite gyms and wellness programs

- Extensive relocation packages (outside a 50 mile radius)

**Additional Details**

**Directive 206.2 **- Employment with Triad requires a favorable decision by NNSA indicating employee is suitable under NNSA Supplemental Directive 206.2. Please note that this requirement applies only to citizens of the United States. Foreign nationals are subject to a similar requirement under DOE Order 142.3A.

**Clearance ****: Q **(Position will be cleared to this level). Selected applicants will be subject to a background investigation conducted by or on behalf of the Federal Government, and must meet eligibility requirements* for access to classified matter. This position requires a Q clearance. and obtaining such clearance requires US Citizenship except in extremely rare circumstances. Dependent upon the position, additional authorization to access classified information may be required, which may or may not be available to dual citizens. Receipt of a Q clearance and additional access authorization ultimately is a decision of the Federal Government and not of Triad.

- Eligibility requirements: To obtain a clearance, an individual must be at least 18 years of age; U.S. citizenship is required except in very limited circumstances. See DOE Order 472.2 for additional information.

**New-Employment Drug Test: ** The Laboratory requires successful applicants to complete a new-employment drug test and maintains a substance abuse policy that includes random drug testing. Although New Mexico and other states have legalized the use of marijuana, use and possession of marijuana remain illegal under federal law. A positive drug test for marijuana will result in termination of employment, even if the use was pre-offer.

**Internal Applicants: **Regular appointment employees who have served the required period of continuous service in their current position are eligible to apply for posted jobs throughout the Laboratory. If an employee has not served the required period of continuous service, they may only apply for Laboratory jobs with the documented approval of their Division Leader. Please refer to Policy Policy P701 for applicant eligibility requirements.

**Equal Opportunity: **Los Alamos National Laboratory is an equal opportunity employer. All employment practices are based on qualification and merit, without regard to protected categories such as race, color, national origin, ancestry, religion, age, sex, gender identity, sexual orientation, marital status or spousal affiliation, physical or mental disability, medical conditions, pregnancy, status as a protected veteran, genetic information, or citizenship within the limits imposed by federal, state, and local laws and regulations. The Laboratory is also committed to making our workplace accessible to individuals with disabilities and will provide reasonable accommodations, upon request, for individuals to participate in the application and hiring process. To request such an accommodation, please send an email to applyhelp@lanl.gov or call (505)-664-6947.

Space Physics Instrumentation and Data Analysis Postdoctoral Researcher

4DMT is a clinical stage biopharma company inventing and developing innovative products to unlock the full potential of genetic medicine to treat large market and rare diseases. Our vector discovery platform Therapeutic Vector Evolution harnesses the power of directed evolution, a Nobel Prize-winning technology, with approximately one billion synthetic AAV capsid-derived sequences to invent customized and evolved vectors with improved therapeutic profiles compared to wild-type vectors. Our product design, development and manufacturing engine empowers us to efficiently create our valuable and diverse product pipeline. This combination of bold innovation and relentless execution gives 4DMT the capability to revolutionize genetic medicines and to strive for potential curative therapies. We have built a deep portfolio of genetic medicine product candidates, with five product candidates in clinical trials for seven patient populations.

We are taking genetic medicine to new heights and into new disease areas to overcome challenges not addressed by existing medicines. This incredible challenge drives our relentless and talented team. Our people are the essence of our inspiring, innovative and collaborative environment that encourages individual contributions and provides opportunities for career development. We seek the best in the industry who identify with our mission and our bold and innovative results-driven approach. Our 4 Guiding Principles drive the way we work together: 
-	Dare to Cure
-	Break Boundaries 
-	Beyond Yourself 
-	Prepare & Executive Relentlessly 

Join us in creating the future of genetic medicine.

Industry: Biotechnology Research
Company Size: 51-200 employees

4D Molecular Therapeutics

**Attention recruitment agencies: **~~All agency inquiries are vetted through 4DMT’s internal Talent Acquisition team. No unsolicited resumes will be accepted. The 4DMT Talent Acquisition team must expressly engage agencies on any requisition. Agencies contacting hiring managers directly will not be tolerated, and doing so may impact your ability to work with 4DMT in the future.~~

4DMT is a leading late-stage biotechnology company advancing durable and disease-targeted therapeutics with potential to transform treatment paradigms and provide unprecedented benefits to patients. The Company’s lead product candidate 4D-150 is designed to be a backbone therapy forming the foundation of treatment of blinding retinal vascular diseases by providing multi-year sustained delivery of anti-VEGF (aflibercept and anti-VEGF-C) with a single, safe, intravitreal injection, which substantially reduces the treatment burden associated with current bolus injections. The Company’s lead indication for 4D-150 is wet age-related macular degeneration, which is currently in Phase 3 development, and second indication is diabetic macular edema. The Company’s second product candidate is 4D-710, which is the first known genetic medicine to demonstrate successful delivery and expression of the CFTR transgene in the lungs of people with cystic fibrosis after aerosol delivery

**GENERAL SUMMARY:**

This role is in the Biomarkers & Immunology department and supports immunogenicity risk assessments, biomarker measurements, and clinical pharmacology deliverables by developing novel bioanalytical methods and providing expert analysis and interpretation of key bioanalytical datasets. Bioanalytical methods are rigorously qualified and validated to generate high-quality data for internal stakeholders. Working closely with cross-functional teams (e.g., Early-Stage Product Development, Project Management, Clinical Operations, and Clinical Development), these deliverables inform key program decisions.

This position reports to the Director, Biomarkers & Immunology, and supports 4DMT’s mission and portfolio of targeted genetic medicines. On-site work is required for laboratory activities; however, a flexible hybrid schedule may be accommodated for data analysis and remote oversight of partner organizations.

**MAJOR DUTIES & RESPONSIBILITIES:**

- Provide scientific and technical leadership in the development and qualification of innovative bioanalytical assays, including ligand-binding assays, anti-drug antibody (ADA) assays, cell-based assays, and molecular assays to evaluate immunogenicity, PK/PD, and biomarkers for preclinical and clinical use across multiple therapeutic areas (e.g., ophthalmology, pulmonology, CNS).

- Lead assay lifecycle activities (method development, qualification, validation, and implementation), including defining fit-for-purpose performance criteria, identifying risks, and driving timely resolution of technical issues.

- Oversee GxP workflows and apply relevant regulatory guidance for early-stage and late-stage assay development, validation, and implementation. Ensure data integrity and inspection readiness as applicable.

- Independently design and execute experiments; analyze and interpret data; and communicate conclusions, limitations, and recommendations to management and study teams to enable decisions.

- Contribute to the design and interpretation of in vivo and in vitro studies to support assay development and biomarker strategy, including selection of appropriate readouts and defining decision criteria.

- Assess and select contract research organizations (CROs), lead technology transfer, and manage external assay method development, qualification, and GxP validation, including vendor performance, issue escalation, and corrective actions.

- Partner with Clinical Development and Clinical Operations to define bioanalytical strategy (including sampling strategy and assay performance characteristics) that supports key clinical pharmacology questions (PK/PD, exposure–response, dose selection).

- Review and interpret bioanalytical datasets for quality, trends, and consistency; summarize findings for study teams and contribute to data summaries.

- Author and/or review sections of clinical and regulatory documents (e.g., protocols, sample handling instructions, bioanalytical plans, study reports, Investigator’s Brochure, IND/CTA content) related to PK/PD, immunogenicity, and bioanalytical methods, ensuring scientific accuracy and consistency of key messages.

- Mentor junior staff by providing technical guidance, coaching on experimental design and data interpretation, and reviewing draft deliverables.

- Maintain awareness of relevant scientific literature and emerging technologies; recommend and pilot improvements that increase assay robustness, throughput, or interpretability.

- Write study reports and manuscripts and present results at scientific meetings.

- Maintain compliance with company Environmental Health and Safety policies, procedures, and practices.

- Contribute to a culture of continuous improvement and innovation; encourage team members to expand technical skills and deepen gene therapy expertise.

**QUALIFICATIONS:**

Education:

- Degree in immunology, bioengineering, molecular biology, cell biology, pharmacology, biochemistry, or a related field.

- PhD with 3+ years of industry or relevant academic experience; Master’s degree with 5+ years; Bachelor’s degree with 7+ years.

Experience:

- Bioanalytical and/or biomarker assay development experience is strongly preferred.

- Experience leading anti-drug antibody assay development and qualification and contributing to validation in a regulated environment (e.g., GxP, as applicable), including defining fit-for-purpose criteria, ensuring data integrity, and troubleshooting complex technical issues. Experience with PCR, qPCR, and droplet digital PCR; RNA-seq; and tissue culture of primary cells and established cell lines. Familiarity with ligand binding assays and LC-MS is a plus.

- Late-stage clinical trial experience, biologics license application experience, and CRO oversight (including deliverable review, issue escalation, and corrective actions) are a plus.

- Working knowledge of clinical pharmacology concepts (PK/PD, exposure metrics, dose selection, exposure–response) and experience translating study objectives into bioanalytical strategy (e.g., sampling strategy, assay performance characteristics), data generation plans, and interpretation for biologics and/or gene therapies is preferred.

Other Qualifications/Skills:

- Competence in standard microplate reader use (e.g., SoftMax software), Meso Scale Discovery platform instruments, PCR primer/probe design, and protein labeling, detection, and purification techniques.

- Demonstrated ability to independently design, develop, and execute new assay methods and to provide technical leadership through critical review of experimental plans, data quality, and conclusions.

- Strong attention to detail with the ability to rigorously analyze and interpret data, ensure data integrity and inspection-ready documentation as applicable.

- Demonstrated ability to influence cross-functional decisions by identifying bioanalytical risks, proposing mitigation plans, and aligning stakeholders on fit-for-purpose approaches.

- Ability to work cooperatively in a team-based environment, supportive of multiple viewpoints and approaches, and able to provide constructive scientific feedback.

- Strong written and verbal communication skills, with demonstrated ability to frame complex data into clear recommendations for diverse audiences (e.g., study teams, functional leaders, and external partners).

- Ability to translate assay performance (e.g., sensitivity, selectivity, drug tolerance, stability, dilutional linearity) into fit-for-purpose guidance for clinical and nonclinical analyses.

- Familiarity with data workflows and common analysis/reporting tools used to summarize and trend bioanalytical results (e.g., Excel, JMP, GraphPad Prism; Python and/or R is a plus).

Travel: <5%

Physical Requirements and Working Conditions:

- Ability to lift up to 20 lbs; bend and twist; and wear personal protective equipment (PPE) such as a lab coat, goggles/glasses, and nitrile gloves.

Base salary compensation range:$164,000 -182,000

4DMT provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, genetic information, marital status, status as a covered veteran, and any other category protected under applicable federal, state, provincial and local laws.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Senior Scientist

Cleveland Diagnostics has unlocked the diagnostic power of protein structure with its revolutionary IsoClear™ platform to develop novel diagnostics based on protein structure-based assessment.

Industry: Biotechnology Research
Company Size: 51-200 employees

Cleveland Diagnostics

**Senior Scientist, IVD Test Dev. **

We are seeking a highly skilled **Senior Scientist, IVD Test Development t **o lead in-vitro diagnostic assay development and validation programs within a regulated environment operating under design control. The successful candidate will provide scientific and strategic leadership for complex projects, driving assay innovation and overseeing verification and validation activities in support of regulatory submissions including PMA, 510(k), and IVDR.  **Title: **  Senior Scientist, IVD Test Development **Location: ** On-site, Cleveland, Ohio **Reports to: ** Sr Director, IVD Test Development  **Job Description: **This role requires deep technical expertise in assay development, experimental design, and advanced data analysis, with responsibility for managing to cross-functional project timelines, technical risk mitigation, and study execution from concept through regulatory submission while collaborating cross-functionally with R&D, Quality, Regulatory, and Manufacturing teams.  The Senior Scientist will define validation strategies, oversee study execution under the company's quality management system, interpret complex datasets, and author and approve technical documentation in compliance with applicable regulatory and quality standards.  In addition to hands-on laboratory oversight, this position will mentor and develop junior scientists, provide technical leadership across teams, and contribute to departmental strategy, process improvements, and long-term product development initiatives. This role may involve handling human biological specimens including blood, plasma, urine, and other bodily fluids, in compliance with all safety regulations and company policies. **Essential Duties and Responsibilities **

- Lead and own complex assay development and validation studies supporting regulatory filings across multiple projects or assay platforms.

- Define study objectives, validation strategies, experimental designs, and success criteria aligned with program goals and regulatory expectations.

- Develop, review, and approve study protocols ensuring scientific rigor and compliance with design control and regulatory agency requirements.

- Oversee execution of product development and validation activities within the company's quality management system.

- Perform or direct complex statistical analyses independently or in collaboration with statisticians.

- Critically interpret experimental data, draw scientifically sound and defensible conclusions, and define strategic next steps to advance programs.

- Identify technical and regulatory risks and proactively develop mitigation strategies to maintain project timelines and compliance.

- Author, review, and approve high-quality technical reports and validation documentation suitable for regulatory submission.

- Develop and deliver data-driven presentations for internal leadership and external stakeholders.

- Lead technical discussions, cross-functional project meetings, and scientific decision-making forums.

- Mentor and develop junior staff, setting expectations for scientific rigor, documentation quality, and regulatory compliance.

- Model and enforce compliance with all safety, biosafety, quality, and company policies.

- Other duties as assigned

**Qualifications/Requirements **

- Bachelor's degree in Biology, Biochemistry, Molecular Biology, Biomedical Engineering, or a related field with 16-20 years of relevant experience.

- Master's degree with 10-15 years of experience.

- Ph.D. with 7-12 years of experience.

**Technical Skills: **

- Extensive technical and managerial expertise developing regulated IVD products

- Deep understanding of CLSI standards and demonstrated ability to design statistically robust analytical validation strategies (precision, linearity, method comparison, LoB/LoD/LoQ, interference, stability) aligned with regulatory expectations.

- Experienced at creating protocols and reports suitable for regulatory submission

- Strong understanding of FDA and global regulatory requirements

- Experience with statistical analysis software (Analyze-It, JMP)

- Commercial IVD product development experience preferred

**Leadership & Analytical Skills: **

- Demonstrated ability to lead research teams and manage multiple projects effectively.

- Strong data analysis and statistical interpretation skills.

- Ability to troubleshoot complex technical issues and drive problem-solving initiatives.

**Communication & Collaboration: **

- Proven ability to develop high-impact scientific reports, publications, and presentations.

- Excellent verbal and written communication skills, with experience presenting to diverse audiences.

- Strong interpersonal skills for mentorship and cross-functional collaboration.

**Physical Requirements/Working Conditions/Equipment Used: **

- Fine motor skills and manual dexterity to handle specimens and lab equipment required to process specimens, troubleshoot and repair instrumentation.

- Visual acuity to examine specimens and reagents

- Offices reachable by elevator but should be able to climb stairs if needed

- Light lifting may be required (up to 25 pounds)

- May be required to stand for long periods of time

- Ability to operate a computer and other technology related lab equipment through course of day

- Ability to work in an environment with exposure to hazardous chemicals and biohazards

- Ability to comply with all appropriate job PPE requirements

- General office and HVAC noise

**Other Requirements **

- Full-time on-site position; this is not a remote position

- This position is classified as exempt and may require work in excess of 8 hours per day and/or 40 hours per week as business needs dictate

- This position may require occasional travel (

Senior Scientist, IVD Test Dev.

**Job Description**

**Job Description:**

We seek a highly motivated and skilled chemist as a Senior Scientist to join our Labeled Compound Synthesis (LCS) group within the Discovery Process Chemistry organization located at our Rahway, NJ site. This role offers the opportunity to join a unique group of innovative laboratory scientists focused on synthesizing isotopically labeled compounds, essential to support drug discovery and development, and developing novel isotope labeling methodologies to enable and speed up and accelerate drug discovery and development. As a Senior Scientist, you will work on collaborative teams to design and synthesize stable and radioactive isotope-labeled drug candidates and metabolites using modern organic synthesis, analytical methods, and emerging technologies. We seek a motivated chemist who will become a subject-matter expert in isotopically labeled compound synthesis—including GMP synthesis for human ADME studies—and who demonstrates strong practical skills in complex molecule design, laboratory instrumentation, and problem solving. Creativity and adaptability are required to develop new labeling approaches, along with self‑initiative, attention to detail, and project planning skills. Excellent interpersonal ability to share specialist knowledge in multidisciplinary teams is essential. If you are passionate about synthetic organic chemistry and thrive in a dynamic environment, we encourage you to apply.

**Education Minimum Requirement**

- A Ph.D. in Chemistry, Pharmaceutical Sciences, or a closely related field achieved no later than June 2026.

Or

- M.S. in Chemistry, Pharmaceutical Sciences, or a closely related field with at least 3 years of industrial/ pharmaceutical experience.

Or

- B.S. in Chemistry, Pharmaceutical Sciences, or a closely related field with at least 5 years of industrial/pharmaceutical experience

**Qualifications**

- Extensive knowledge and experience with modern methods of organic synthetic chemistry.

- Skilled in analytical and purification techniques (including chromatography and crystallization)

- Good organizational, interpersonal, writing, and time management skills.

- Keen attention to detail and ability to author clear reports and review the reports of others.

- Ability to strictly follow established procedures, policies, and guidelines required to comply with safety/radiation safety, environmental, and GMP expectations in the lab.

- Demonstrated ability to develop, apply, and/or improve new workflows and best practices.

- Demonstrated ability to design and conduct experiments, generate and analyze data, properly dispose of waste, and work effectively in a dynamic environment.

**Preferred Experience And Skills**

- Experience working with stable and/or radioactive isotopes is desirable but not required.

- Experience with the synthesis of large molecules (peptides, RNAs, ADC-conjugates, etc.) is desirable but not required

- undefined.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

**Required Skills**

Accountability, Adaptability, Biopharmaceuticals, Chemical Synthesis, Chromatography, Data Analysis, Data-Driven Decision Making, Detail-Oriented, Emerging Technologies, GMP Compliance, Healthcare Innovation, Machine Learning (ML), Motivation Management, Organic Chemistry, Organic Synthesis, Time Management

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.

**Requirements**

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

**U.S. Hybrid Work Model**

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$117,000.00 - $184,200.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

**San Francisco Residents Only: ** We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

**Los Angeles Residents Only: ** We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

**Search Firm Representatives Please Read Carefully**

Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

1st - Day

**Valid Driving License**

No

**Hazardous Material(s)**

Yes

**Job Posting End Date**

04/25/2026

- A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.

**Requisition ID: **R392202

Senior Scientist, Chemistry - Onsite

e184 is an Advanced Research Funding Organization (ARFO) that supports frontier science and technology.

We are living in an exponential age. The challenge is that humans are not used to it. Our skills and capabilities are not growing at an ever-increasing rate, and even the population growth rate has slowed down, failing to align with an exponent. At e184, our mission is to invest in science and technology that transforms humans into exponential species.

Industry: Venture Capital and Private Equity Principals
Company Size: 2-10 employees

e184

**About us **

e184 Artificial Womb is a biotechnology research company dedicated to advancing ectogenesis - the ability to support human development outside the body - to expand reproductive freedom and redefine what is possible in medicine. Our mission is to remove the biological constraints that limit who can safely carry a pregnancy, enabling new pathways to parenthood for individuals facing medical risk, infertility, or physiological barriers to gestation.

We operate at the intersection of biology, engineering, and computational science, building integrated platforms that combine advanced tissue models, adaptive culture systems, and automated experimental workflows to understand and recreate the conditions required for healthy human gestation beyond the uterus.

**Role overview **

As a Senior Scientist at e184 Artificial Womb, you will lead research focused on translating in vivo placental biology into experimentally tractable model systems that inform the development of functional placental platforms for ex utero gestation. Your work will center on applying mechanistic understanding of placental development, structure, and maternal–fetal exchange to guide the design and optimization of placental organoid and co-culture models capable of supporting perfusion and sustained fetal development.

You will drive experimental strategy from biological discovery through model validation, working closely with tissue engineers, biomaterials scientists, and perfusion engineers to integrate placental biology into engineered systems. This is a highly hands-on leadership role for a scientist with deep expertise in placental development who is excited to translate fundamental reproductive biology into next-generation experimental platforms within a fast-moving, interdisciplinary startup environment.

**What you´ll do **

- Translate in vivo placental biology: Apply knowledge of placental development, trophoblast differentiation, and maternal–fetal exchange to define biological requirements for engineered placental systems.

- Develop placental organoid models: Establish and optimize placental organoid and co-culture systems that recapitulate structural, cellular, and signaling features of developing placenta.

- Guide functional platform development: Inform the design of perfusion-compatible models that enable nutrient, gas, and signaling exchange required for sustained fetal development.

- Characterize placental structure and function: Use imaging, histology, molecular profiling, and functional assays to evaluate trophoblast differentiation, vascular interactions, and transport capacity.

- Define developmental signaling environments: Identify molecular pathways and extracellular cues that regulate placental maturation and integrate findings into experimental platform design.

- Drive interdisciplinary collaboration: Work closely with tissue engineering, hydrogel, and perfusion teams to translate biological insight into engineered solutions supporting long-term development.

**Core requirements **

- PhD in Placenta Biology, Developmental Biology, Reproductive Biology, Cell Biology, or a related field with postdoctoral experience, or 7+ years of relevant industry or academic experience

- Demonstrated expertise in placental development and trophoblast biology

- Strong understanding of maternal–fetal interface biology and placental physiology

- Hands-on experience with mammalian cell culture and placental model systems

- Experience designing and executing independent experimental research programs

- Familiarity with histological and molecular approaches for studying placental development

- Ability to lead complex interdisciplinary research efforts

- Strong organizational and documentation skills

- Comfort working in a fast-paced, iterative startup environment

**You´ll stand out with **

- Experience developing or working with placental organoids or advanced in vitro placental models

- Expertise in trophoblast stem cell biology and differentiation

- Experience studying placental vascularization or nutrient transport mechanisms

- Hands-on histology experience, including tissue processing, sectioning, staining, and microscopy-based analysis

- Experience with transcriptomic, single-cell, or spatial omics approaches in developmental systems

- Familiarity with perfusion or microphysiological culture platforms

- Experience translating in vivo biological findings into engineered or experimental systems

- Prior startup or early-stage technology development experience

**Why e184? **

- Unrivaled impact: Your work directly enables technology that transforms human fertility and reproductive medicine.

- Full-spectrum growth: Gain exposure to the entire lifecycle of discovery. From screening to mechanistic validation.

- Best of both worlds: Experience the creative chaos of an early-stage startup with the stability of a well-capitalized company.

- Elite collaboration: Work alongside a world-class team who are as driven as you are.

**What we offer **

- Competitive salary + equity participation is considered

- State-of-the-art facility in Portland metro area

- Comprehensive Medical, Dental, Vision, and 401(k) with company match

- 20 days PTO + 11 paid holidays

Senior Scientist - Placenta Biology

Pay is commiserate with experience and ranges between $42-52/hr

Scientist, III – Biocompatibility, Tissue Material Sciences (Contractor)

**Job Summary**

The Senior Scientist I - Biocompatibility is a SME related to the biocompatibility and nonclinical safety evaluations of medical devices, biomaterials, tissue products, and combination products as a part of R&D. This individual must possess an extensive knowledge of ISO-10993 Standards and prior experience working in biocompatibility. The position will be responsible for cross-functional and cross-site collaborations and recommendations of biocompatibility activities, including establishing requirements, planning, execution and approval of biocompatibility requirements in support of regulatory submissions, project teams, operations, with a large focus on manufacturing and change control (product support).

KEY DUTIES AND RESPONSIBILITIES: DESCRIBE SCOPE:

-  Function as Subject Matter Expert for ISO-10993 (biocompatibility) assessment management with minimal supervision. This will include the design, execution and interpretation of biocompatibility evaluation strategies and programs according to relevant regulatory requirements, including biological risk assessments, technical reports, technical memoranda and other documents for internal and external distribution, including regulatory submissions.

-  Responsible for creating detailed Project Plans including scientific strategy and realistic deliverables with timelines. Actively involved in the planning, execution and management of experimental studies for the safety characterization of novel and existing products.

-  May serve as a sub-team or core-team member, providing support as needed for all project Teams.

-  Support for on-market products, including global change-control activities as they relate to biocompatibility. Requires interacting with Manufacturing Sites.

-  Maintain knowledge of medical device regulations to assure compliance and conformance of programs for evaluation of medical device and other products. This includes performing gap analysis relevant to changes in biocompatibility standards or guidance.

-  Prepare and deliver technical presentations to internal and external stakeholders with minimal supervision. Assist the team in functional training initiatives.

-  Build and maintain strong connections and relationships with Contract Research Organizations, Toxicologists and Consultants for Biological Risk Assessments as needed.

Education and Experience

-  Bachelor’s Degree in Life Science/Biomedical Engineering or related field with minimal 6 years of experience in a scientific role in the medical device or pharma industry or Master’s degree (with thesis) in Life Science/Biomedical Engineering or related field with at least 4 years of experience in a scientific role in the medical device or pharma industry.

-  Medical device, pharmaceutical or related experience or experience in a regulated environment with a proven record of success supporting patient safety studies for R&D projects is preferred.

-  Significant experience and knowledge of medical device and combination product regulations

-  Strong knowledge of ISO-10993 Standards, FDA Guidance and Regulations, and Animal Welfare Regulations.

-  Strong technical writing and verbal communication skills.

-  Experience managing outsourced contract research (GLP, non-GLP, GMP activities).

-  Strong familiarity with the product development process for medical devices or biologics

-  Demonstrate critical thinking and problem-solving skills, including analysis and presentation of data.

-  Self-motivated and proactive; ability to execute with minimal supervision and direction. Can work independently or part of a team.

-  Ability to communicate complex technical information in a clear and easy-to-understand way (both verbally and in writing).

-  Author internal reports and procedures as well as collaborating on manuscripts and abstracts for external submissions.

-  Knowledge of Good Documentation Practices, maintain accurate documentation & related record retention documentation.

-  Knowledge of Good Laboratory Practices (21 CFR, Part 58) and ISO-10993 standards .

-  Proficient in required software including Word, Excel, PowerPoint, and Outlook, and statistical software

Senior Scientist I - Biocompatibility

Job Title: REACH Scientist

Location: Naugatuck, CT

Zip Code: 06770

Pay Rate: $52.00/hr

Keyword's: #Naugatuckjobs; #Scientistjobs.

Start Date: Immediate

Job Description:This position provides clear opportunity for analytical scientific creativity for developing separations, determining ionization and analysis parameters, interpretation of results, and aligning with other scientists for data/report compilation. The analysis of complex mixtures inherently provides complexity to the task.

Skills/Experience: * Required Education & Experience: Ph.D. or equivalent, 5+ years' experience or BS/MS + 10 years' experience.

* Required Years of Professional Experience: >10 years

* Strong written and oral communication skills including live presentation.

* Advanced expertise in various types of Mass Spectrometry.

* Basic expertise in Lubricant chemistry is a plus.

Since 1988, PSI teams have provided our government customers with innovative, cost effective solutions that solve today’s complex challenges, improve operational efficiencies, and meet challenges to our national security. PSI provides expertise across a broad spectrum of capabilities ranging from Cyber Security to Cloud Migration, Systems Engineering, Augmented/Mixed Reality, and DevSecOps.    

Mission: To provide value-added information technology and management consulting services and solutions while consistently delivering success to our customers.

Vision: To be recognized as a world-class provider of innovative solutions that benefit our customers through a relentless commitment to our core values of people, service, and integrity.

People – We operate in a climate of trust, respect, empowerment, teamwork and cooperation.
Service – We conduct ourselves with unfailing commitment to our customers' success.
Integrity – We are honest, open, and ethical in everything we do.

Industry: IT Services and IT Consulting
Company Size: 1,001-5,000 employees

Planned Systems International

Planned Systems International (PSI) is an enterprise IT services company that designs, builds, secures, and operates software solutions that support mission success and operational excellence across Federal Government organizations. PSI is seeking an AMOC Senior Scientist to provide full-time support to the CBP Air and Marine Operations Center.

This role is responsible for applying advanced scientific, analytical, and technical expertise to support C4I systems, ISR capabilities, and data-driven mission operations, including development of innovative approaches to enhance system performance, predictive analysis, and operational effectiveness.

**Essential Functions And Job Responsibilities**

-  Apply scientific and analytical methods to evaluate C4I, ISR, and operational data environments

-  Develop models, simulations, and analytical frameworks to support mission decision-making

-  Support data analysis efforts related to sensor inputs, surveillance systems, and operational intelligence

-  Conduct research and analysis to improve system performance, predictive capabilities, and mission outcomes

-  Provide technical expertise in evaluating emerging technologies and their applicability to mission needs

-  Support development of data-driven solutions for threat detection, situational awareness, and operational planning

-  Collaborate with engineering and operations teams to integrate analytical solutions into operational systems

-  Analyze system performance data and recommend improvements to enhance reliability and effectiveness

-  Support testing, validation, and evaluation of new analytical tools and capabilities

-  Provide technical reports, briefings, and recommendations to Government stakeholders

-  Ensure compliance with security, data handling, and operational requirements

**Minimum Requirements**

-  Bachelor’s degree in Engineering, Computer Science, Information Technology, or related field; experience may substitute

-  Experience supporting maintenance and sustainment of C4I, AMOSS, or ISR systems in operational environments

-  Experience troubleshooting complex system issues across hardware, software, and network components

-  Experience working with mission equipment, maintenance tools, and COTS systems

-  Experience using diagnostic and test equipment to identify and resolve system faults

-  Demonstrated understanding of operational requirements and ability to apply technical procedures in mission environments

-  10+ years:

-  Applying scientific or analytical methods to complex technical or operational problems

-  Supporting ISR systems, data analysis, and C4I environments

-  Developing models, simulations, and analytical tools

-  Analyzing large datasets and generating actionable insights

-  Supporting mission-critical operations in high-tempo environments

-  Working within DoD, DHS, or similar Federal operational environments

**Physical Demands**

-  Ability to work in operational environments supporting technical systems

-  May require standing, walking, and limited lifting of equipment

-  Ability to travel and deploy to operational locations as required

**Additional Information**

-  Travel is required to support mission operations, system maintenance, and engineering activities across CBP operational locations. Personnel will deploy to sites including CAMOC in Aguadilla, Puerto Rico, and other CONUS and OCONUS locations to perform installation, troubleshooting, integration, and sustainment of C4I, AMOSS, ISR, and telecommunications systems. Travel may be scheduled or occur on short notice in response to mission priorities or system outages. Duration may range from short-term temporary duty to extended support periods based on operational needs. All travel will be Government-directed and reimbursed in accordance with applicable Federal Travel Regulations and contract provisions.

**Company Benefits**

PSI offers full-time, benefits eligible employees a competitive total compensation package that includes paid leave, and options for employer sponsored group medical, dental, vision, short-term and long-term disability, life insurance, AD&D coverage, legal services, identity theft, and accident insurance. Flexible spending account and health saving account options offer pre-tax savings for qualified medical, dental, and vision expenses. The company sponsored 401(k) retirement plan has an employer contribution match that is immediately vested. We invest in the professional growth of our employees through professional courses, certifications, and tuition reimbursement programs.

**EEO Commitment**

It is company policy to promote equal employment opportunities. All personnel decisions, including, but not limited to, recruiting, hiring, training, promotion, compensation, benefits, and termination, are made without regard to race, color, religion, age, sex, sexual orientation, pregnancy, gender identity, genetic information, national origin, citizenship status, veteran status, protected veteran status, disability, or any other characteristic protected by applicable federal, state, or local law.

Reasonable accommodations for applicants and employees with disabilities will be provided. If a reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact Human Resources by emailing HRDepartment@plan-sys.com , or by dialing 703-575-8400.

AMOC Senior Scientist

Novara™ delivers next-generation thermal, protective, and adaptive materials that integrate seamlessly into products, elevating performance from the inside out.

Started on the Ohio State University tech campus, Novara™ has partnered with science and technology leaders to evolve the idea of heat anywhere.

Industry: Nanotechnology Research
Company Size: 2-10 employees

Novara Materials

**Job Overview **

Assists in the research, development, and characterization of heated film technologies utilizing nanomaterials. Performs routine laboratory work, including material preparation, testing, and data analysis under the guidance of senior scientists and engineers. Supports the development of innovative heating solutions by applying knowledge of materials science and chemistry to real-world product challenges.

**Responsibilities **

- Assist in the formulation, processing, and characterization of materials used in thin-film heater development.

- Prepare and evaluate polymer films, conductive inks, adhesives, and dispersion systems for electrical and thermal performance.

- Conduct laboratory experiments and document results accurately, maintaining thorough lab notebooks and test records.

- Support the development of screen-printing processes for the deposition of conductive materials.

- Perform material testing, including thermal analysis, resistivity measurements, adhesion testing, and environmental exposure testing.

- Assist in troubleshooting material and process issues during product development and scale-up activities.

- Collaborate with engineering teams on design reviews, process validations, and corrective actions.

- Maintain laboratory equipment in proper working order and ensure safe handling of chemicals and materials.

- Prepare technical summaries, test reports, Invention Reports, and IP-related documentation

**Other Items: **

- Follow all corporate expectations and company policies.

- Maintain a safe and clean work area and comply with all laboratory safety protocols.

- Work with and have functional knowledge of computer systems, laboratory instrumentation, and data analysis tools.

- Note that this job description may not cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job.

- Duties, responsibilities, and activities may change at any time with or without notice.

- Up to 15% travel may be required to support vendor activities and product production.

**Qualifications **

- B.S. degree in Materials Science, Chemistry, Chemical Engineering, or a related technical field is required.

- 1–2 years of relevant laboratory or industry experience; internship or co-op experience in a manufacturing or R&D environment is a plus.

- Familiarity with polymer films, adhesives, or coating technologies is a plus.

- Experience with material characterization techniques (e.g., SEM, TGA, DSC, four-point probe, tensile testing) preferred.

- Ability to work independently or as part of a team in a fast-paced start-up environment

- Strong attention to detail and commitment to accurate data recording and reporting.

- Strong communication skills, both written and verbal.

- Knowledge of ISO standards or laboratory quality systems is a plus.

Material Scientist I

At Joulé, we believe our world is filled with possibilities – where character, integrity, and commitment drive our purpose. For over 30 years, Joulé has been a trusted partner to industry-leading clinical, scientific, and healthcare organizations by providing innovative workforce solutions and delivering top talent. Operating at the forefront of the life sciences arena, Joulé’s relentless approach enables our clients to rapidly and effectively execute critical initiatives and major projects. Joulé is a System One division.

Industry: Staffing and Recruiting
Company Size: 51-200 employees

Joulé

**Job Title: ** Senior Scientist: Cheminformatics & Computational Chemistry

**Location: ** South San Francisco, CA (Hybrid; remote considered case-by-case)

**Hours: **M-F, 8-5

**Type: ** 7-month contract

**Compensation: **$80 - 90/hr (depending on qualifications)

OverviewThe Cheminformatics Senior Scientist will design and implement end-to-end computational workflows to support small molecule drug discovery within the TuneLab platform. This role is ideal for a highly technical scientist who can independently evaluate tools, integrate advanced modeling approaches, and deliver scalable, production-ready solutions. You will operate at the intersection of cheminformatics, physics-based simulation, and machine learning in a fast-moving, high-impact environment.

Responsibilities

- Design and implement end-to-end workflows spanning virtual screening, hit identification, hit expansion, and lead optimization.

- Develop and integrate ligand-based and structure-based modeling approaches, including QSAR, docking, and pharmacophore modeling.

- Execute ultra-large library searches using substructure, similarity, and embedding-based methods.

- Build molecular enumeration pipelines using reaction-based and fragment-based design strategies.

- Apply physics-based simulation methods such as molecular dynamics (MD) and free energy perturbation (FEP).

- Evaluate computational tools and make build-versus-buy decisions for workflow components.

- Collaborate with machine learning teams to integrate predictive and generative models into workflows.

- Partner with software engineering teams to productionize workflows and ensure scalability and performance.

- Align computational strategies with scientific and drug discovery objectives through cross-functional collaboration.

RequirementsMust Have

- PhD or MS in Cheminformatics, Computational Chemistry, Medicinal Chemistry, or a related field.

- Strong understanding of small molecule drug discovery workflows.

- Demonstrated expertise in:

Substructure and similarity search (fingerprint-, graph-, or embedding-based)Shape and pharmacophore screeningReaction-based and fragment-based enumerationDocking and structure-based designQSAR and ligand-based modelingActive learning and iterative design strategiesPhysics-based simulations (e.g., MD, FEP)

- Hands-on experience with cheminformatics and modeling tools such as RDKit, OpenEye, or similar.

- Experience with docking platforms (e.g., Glide, AutoDock, GOLD).

- Strong programming skills in Python.

- Ability to work independently and apply scientific judgment to complex problems.

Nice to Have

- Experience working with ultra-large chemical libraries (e.g., Enamine REAL, WuXi Galaxy).

- Familiarity with generative chemistry approaches (SMILES-, graph-, or diffusion-based models).

- Experience integrating machine learning models into production workflows.

- Experience with workflow orchestration tools such as Airflow or Nextflow.

BenefitsSystem One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

#M-

Ref: #558-Scientific

Cheminformatics Senior Scientist

BioSpace is the digital hub for life science news and jobs. We provide essential insights, opportunities and tools to connect innovative organizations and talented professionals who advance health and quality of life across the globe.

Industry: Internet News
Company Size: 11-50 employees

BioSpace

**Company Description**

**About AbbVie**

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

**Job Description**

AbbVie Discovery Neuroscienceteamseeksacollaborativesenior scientistwho willlead fromthe laboratory benchto support advancement of psychiatry assets.In this onsite role,youwillleverageyoursignificant demonstrated experience inmolecular and cellular pharmacology,in vitrohuman-derivedcellular models, and ex vivo sample analysistopropose/evaluatenew approachesandcarry outwell-matched approachesfor scientific questionssupporting advancement of assets through stage-gate transitions.

You will be expected tohavestrong communicationskills,be agile,operatecomfortably with ambiguity on formal and informal teams, and workwith a sense of urgency and accountability to advance projects efficientlyand compliantly.Opportunities will exist tocontribute to target validationand progression,collaborate across AbbVie sites,presentyour work,and mentor scientists.Wereexcited to see how you canhelpAbbViedeveloplife-changing psychiatric therapeutics for patients.

**Responsibilities**

- Proactively translatedepartment/projectteam scientific questions into well-designed experiments,utilizinginternal and external resources

- Exploremultipletechnicaloptions forapproach,quality, feasibility,efficiencyand present recommendations atprojectteam or group meetings

- Set upand carry outnovelmolecular and cellular assays/modelstosupport SAR and understanding of target biology in context of project team goals & transitions

- Document protocols and results in databases and electronic laboratory notebook, contributing to formal study reports per business need

- Upholdimpeccableresearch-related&corporate compliancestandards

- Collaborateacross the organization;Mentor/matrix managejunior scientists

**Qualifications**

- Bachelors Degree or equivalent education and typically 12+ years of experience, Masters Degree or equivalent education and typically 10+ years of experience, PhD and typically 4+ years of experience.

- Possess thorough theoretical and practical understanding of own scientific discipline.

- Effective writer and communicator of research or other regulatory materials.

**Desired Qualifications**

- Significant experiencewithrunning and interpretingpharmacological studies,humaniPSC-neuronculture,clonal cell lineculture, equipment/assayselectionand development

- Growth mindset with strong organizational, communication, and collaboration skills

- Demonstrated ability to learn and master new experimental techniques

- Attention to detail with ability to see big picture,multitask and work within timelines

- Pharmaceutical industrydrug discoveryexperience

- Experiencewith endpoints related toneurotransmitters, receptor signaling, trafficking, neuroplasticity, proteomics.

- Experience withmedium to high throughput technology and techniques such as electronic dispensing equipment/robotics,AlphaLISA, HTRF, ELISA, MSD, qPCR, capillary Western, FLIPR,kinetic/endpoint assays, high-contentimaging; engages vendors/reads manuals

- Ex vivo sampleassay design,processing,andanalysis experience

- Additional CNS iPSC-derived cell experience,encompassing multiple cell types

- Psychiatry therapeutic area experience

- FamiliarityleveragingAI tools to improve productivity

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

- The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this postingbased on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore orless than the posted range. This range may bemodifiedin thefuture.

- We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

- This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.The amount and availability of any bonus,commission,incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paidandmay bemodifiedat the Companys sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

Senior Scientist II, Molecular & Cellular Pharmacology, Discovery Psychiatry

Imperial County is home to approximately 180,000 residents which live and work within its seven cities (Brawley, Calexico, Calipatria, El Centro, Holtville, Imperial and Westmorland) and eight unincorporated communities (Bombay Beach, Heber, Niland, Ocotillo, Palo Verde, Salton City, Seeley and Winterhaven).  The county was the last to be established in California in 1907; however it is the ninth largest California County encompassing 4,284 square miles.

Imperial County has much to offer.  We have a rich agricultural heritage, which includes the production of half of our nation’s winter vegetables, an extensive amount of renewable resources, including geothermal, wind, and solar, a wide-range of cultural and outdoor recreational activities with hundreds of points of interest such as the Imperial Sand Dunes Recreation Area, a magnet for off-road enthusiasts, and the Sonny Bono Salton Sea National Wildlife Refuge, a renowned birding site, and a lively population with frequent family-oriented community events.

Industry: Government Administration
Company Size: 1,001-5,000 employees

County of Imperial

Under the direction of the Public Health Laboratory Manager, perform public health laboratory tests and analysis on clinical, environmental and animal specimens in support of public health programs and community health care providers; provide administrative and technical support for public health programs, supervisors and administrators.

Any combination equivalent to: bachelor’s degree in chemistry, biology, microbiology or other subject area consistent with California certification for registration as a Public Health Microbiologist.

Public Health Microbiologist certificate issued by the California State Department of Health Services.

A valid driver’s license may be required at the time of appointment and employees may also be required to drive their own vehicle and provide proof of liability insurance as per Vehicle Code VC

- 160020. Individuals who do not meet this requirement due to a disability will be reviewed on a case-by-case basis.

This position may require pre-employment drug test, physical examination, and fingerprinting for a background investigation.

The County of Imperial does not unlawfully discriminate on any prohibited basis under state or federal law including prohibitions listed in title VII, the Age and Discrimination and Employment Act, section 504 of the Rehabilitation Act of 1973, the Fair Employment and Housing Act, and the Americans with Disabilities Act.

If you feel you have a need for special arrangements due to a disability in order to participate in the recruitment process, call (442) 265-1148 or TTY (442) 265-1169.

- NOTE: IF YOU BELIEVE YOUR CIVIL RIGHTS IN EMPLOYMENT MATTERS HAVE BEEN VIOLATED AT ANY TIME DURING THE COURSE OF YOUR CONSIDERATION FOR EMPLOYMENT, CONTACT THE EQUAL EMPLOYMENT OPPORTUNITY OFFICE, 940 W. MAIN STREET, SUITE 101, EL CENTRO, CA 92243, PHONE: (442) 265-1017 (DO NOT CALL THIS NUMBER FOR GENERAL EMPLOYMENT OR JOB APPLICATION INFORMATION).

About Imperial County: Imperial County is located in the Imperial Valley in the southeast of California, bordering Arizona and Mexico, with the Colorado River forming the County’s eastern boundary. Imperial County is a major agricultural center, producing half of the nation's winter vegetables, as well as extensive renewable resources, such as geothermal, wind, and solar. Off-road enthusiasts are drawn to the Imperial Sand Dunes Recreation area, and the Colorado River is a popular destination for watersports, including fishing, boating, and water skiing. Fans of the popular movie, The Return of the Jedi, will recognize the Algodones Sand Dunes, where the movie was filmed.

Public Health Microbiologist

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