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

Savvy Admin PROD

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

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.

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

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)

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 **

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)

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

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

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

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

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

**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)

A global leader in applied safety science, UL Solutions transforms safety, security, and sustainability challenges into opportunities for customers in more than 100 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. 

The UL Certification Marks serve as a recognized symbol of trust in our customers’ products and reflect an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. 

We believe in the possibility and promise of innovation, and we have spent more than a century enabling it to be safely adopted. From the adoption of electrification to the enablement of 5G and new mobility, we collectively look toward new frontiers, working for a safer world. Our science is your advantage.

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

UL Solutions

**Job Description**

UL Solutions is a global leader in safety science, providing the expertise and services organizations need to tackle critical business challenges. We help customers meet their safety, security and sustainability goals, manage risk, achieve regulatory compliance and deliver products that meet quality expectations. A Laboratory Chemist will take a hands-on approach in our testing process at our headquarters in Northbrook, IL.

**Responsibilities**

-  Follows defined test plans and datasheets with necessary supervision/support. Evaluates test performance and

sample operation to properly evaluate test results. Records and explains test results and completes test report.

-  Serves as Lead for simple test programs as assigned with the necessary assistance. Communicates project status

and results as needed. Holds responsibility for defining test plan, report completion and accuracy, meeting of agreed

deadlines, and managing project related activities.

-  Examines customer samples and learns to operate appropriate tests for each case with support. Communicates with

internal customers during setup and operation to ensure proper evaluation.

-  Directs, builds and/or adapts simple test setups, sample preparations/solutions and instruments to new situations,

based on test plans and instructions. Trains other lab staff on these test procedures or instruments.

-  Operates and maintains test instruments appropriately to measure and test samples. Performs maintenance on

designated test instruments and laboratory area.

-  For a single testing technology, integrates basic process and instruments improvements into all aspects of the job.

Communicates with management and technical staff to provide suggestions for new instruments, processes, and

forms to improve accuracy and efficiencies.

-  Understands and follows safe chemical hygiene practices.

-  Read and follow the Underwriters Laboratories Code of Conduct, and follow all physical and digital security practices.

-  Other duties as assigned

**Qualifications**

-  Bachelor’s degree or diploma from an accredited university through a formal program of study in Chemistry or related

discipline including Chemical Engineering, Biochemistry, Organic/Inorganic Chemistry, Material Science but not limited

to these disciplines only.

-  Demonstrated ability to manage multiple projects while maintaining high quality and exceptional customer service.

-  Demonstrated ability to successfully partner with Engineering and other Laboratory Personnel to complete projects in

a timely manner with high quality.

-  Demonstrated ability to analyze special testing needs.

-  Effective communication skills and ability to interact with customers

-  Demonstrated ability to be innovative and creative

-  Desire to work in a team-oriented environment

-  Ability to use Microsoft Office suite is a must

-  Ability to incorporate automation into day-to-day testing

**Total Rewards: ** We understand compensation is an important factor as you consider the next step in your career . The estimated salary range for this position is $52,900 to $70,500 and is based on multiple factors, including job-related knowledge/skills, experience, geographical location, as well as other factors. This position is eligible for annual bonus compensation with a target payout of 5% of the base salary. This position also provides health benefits such as medical, dental and vision; wellness benefits such as mental and financial health; and retirement savings (401K) commensurate with the standard rewards offered in each individual location or country. We also provide full-time employees with paid time off including vacation (15 days), holiday including floating holidays (12 days) and sick time off (72 hours).

**About Us**

A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.

**About The Team**

Our global network of 80+ laboratories is constantly evolving, because the world around us is always changing. We embrace this — we invest in improving our equipment and our skills so we’re one step ahead of the market. One day we could be setting up a burn test and the next, simulating a tornado. And because we’re always evolving, your career will evolve alongside us, whether you’re working on brand new technology or connecting with experts around the globe. Join our team, drive the growth of our organization and deliver real change — in a changing world.

Laboratory Chemist

**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

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**

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

Pixelle Specialty Solutions™ is one of North America's largest specialty paper companies, with pulp and paper operations in Spring Grove, PA, Chillicothe, OH, Stevens Point, WI, and a coating operation in Fremont, OH. Pixelle, formerly Glatfelter Specialty Papers, was formed in 2018 by Lindsay Goldberg, a private investment firm that partners with families, founders, and management teams seeking to build their businesses actively. Supported by an experienced product development team, the company excels in designing customized solutions to meet today’s challenging demands.

Industry: Paper and Forest Product Manufacturing
Company Size: 1,001-5,000 employees

Pixelle Specialty Solutions

Role

Using analytical methods and processes, the chemist is responsible to provide technical information across the organization. This includes (but not limited to) initiatives supporting product development, operations, quality, environmental, and safety.

Accountabilities

-  Capable of following standard electronic or written analytical methods and procedures.

-  Ability to develop and document new analytical methods for customer products, final products, raw materials, and process streams, as needed.

-  Ability to read, analyze, and interpret common scientific and technical journals.

-  Ability to define problems, collect data, establish facts, and draw valid conclusions.

-  Laboratory wet chemistry skills.

-  Experience with SEM/EDX and microscopy is the primary responsibility of this position.

-  Experience with the management and support of a laboratory information management system (LIMS) software is a secondary responsibility.

-  Maintenance and management of software to backup data from the various instruments in the department is a plus.

-  Ability to use and learn additional laboratory equipment and techniques, including but not limited to, ICP, IC, Sedigraph, FTIR, GC, GC/MS, HPLC, LC/MS, microscopy, SEM/EDX, DSC/TGA, contact angle, sample preparation techniques (such as: pyrolysis, SPME, extractions, and derivatizations).

-  Ability to perform routine troubleshooting and maintenance on instrumentation utilized.

-  Write detailed reports with analytical findings.

-  Maintain well organized records of all work done, in conformity with departmental practices.

-  Ability to respond to common inquiries or complaints from customers.

-  Ability to work with others on large cross-functional projects, as well as the ability to work independently.

-  Detailed knowledge of safe work practices, as well as proper waste handling/ disposal in the laboratory, etc. Knowledge of environmental and safety regulations as pertains to the pulp and paper industry, is a plus.

**Requirements**

- B.S. in Chemistry.

-  Two (2) or more years’ experience in an analytical lab setting preferred.

-  Must be able to demonstrate ability to handle multiple projects.

-  Computer Skills: word processing, spreadsheets, internet software, e-mail, database software.

-  Excellent communication skills (both written and verbal).

-  Highly self-motivated

Chemist I

IntelliPro Group Inc. is one of the fastest growing IT services and HR solutions companies in Americas & APAC. We provide comprehensive IT services to help clients with IT Strategic Planning, Implementation, Deployment, IT Support on Artificial Intelligence, Big Data, Cloud Computing, Mobile Application Development, Data Mining and Business Intelligence, Enterprise Data Warehouse, and more. 

Besides our established IT services, our new business now is quickly extending to one-stop HR Solution Services, including Oversea Branch Setup Consulting, Compensation & Benefits Policy Consulting, Payroll Management Service, Talent Recruiting, and Employer Branding to satisfy our clients’ fast business expansion requirement.

We have built our business on our company-wide commitment to continually overdeliver on the high expectations of our clients, employees, and business partners. The secret to our success is that our unified team works harder, faster, smarter, and more collaboratively than anyone else in the talent acquisition business. In addition to the immense talent and proprietary technology, IntelliPro Group is proud to offer continual professional development and extraordinary benefits to both consultants and full-time employees.

Industry: Staffing and Recruiting
Company Size: 201-500 employees

IntelliPro

**Job Title: ** Formulation Chemist

**Position Type: **Temp to Full-time

**Location: **Redondo Beach, CA (Onsite)

**Rate: ** $25-35/hr.

**Job ID#: **165428

**Job Description: **

**Position Summary **

The Formulation Chemist I is responsible for preparing routine bulk solutions used in the manufacturing of in vitro diagnostic (IVD) products. This role performs formulation activities in compliance with established procedures and documentation requirements to support the production of high-quality IVD products.

This position offers **long-term growth potential **, with opportunities to expand into broader operational responsibilities and progress into leadership or management roles for high-performing individuals.

The Chemist maintains accurate batch records, ensures organization of the cold room, freezer, and formulation laboratory, and contributes to operational efficiency. This role also supports documentation activities, including writing, reviewing, revising, and updating manufacturing documents and SOPs.

The ideal candidate thrives in a **fast-paced, hands-on manufacturing environment **, demonstrates strong multitasking abilities, and brings a proactive, solutions-oriented mindset while maintaining a safe and compliant workplace.

**Supervision **

Works under minimal supervision.

**Essential Functions & Responsibilities **

- Prepare and execute bulk solution formulations in accordance with established procedures.

- Perform hands-on manufacturing activities, including handling materials and supporting production operations (lifting, pulling, and movement of materials as needed).

- Assist with raw material qualification, in-process checks, and formulation-related CAPAs or nonconformances (NCs).

- Review and maintain accurate batch records and formulation documentation.

- Organize and maintain the cold room, freezer, and formulation laboratory for optimal efficiency.

- Write, review, revise, and update manufacturing documents, SOPs, and other technical documentation.

- Support departmental inventory management activities.

- Participate in process improvement initiatives and continuous quality enhancement efforts.

- Ensure compliance with applicable GMP, ISO 13485, and internal quality system requirements.

- Contribute to a safe, positive, and collaborative work environment.

- Perform additional duties as assigned by management.

**Education & Experience **

- Associate degree in Chemistry, Biology, or a related field with a minimum of three (3) years of relevant laboratory or manufacturing experience in a GMP or IVD environment; OR

- Bachelor’s degree in Life Sciences, Biology, Biochemistry, or related field with a minimum of one (1) year of relevant experience; OR

- Equivalent combination of education and experience.

**Additional Requirements: **

- Candidates must have **prior hands-on work experience **.

- **Formulation experience is preferred but not required **; strong manufacturing experience in large-scale environments is highly valued.

**Skills, Knowledge & Abilities **

- Knowledge of solution chemistry and basic formulation principles.

- Experience in **manufacturing environments with high workload demands **, including physical tasks.

- Strong understanding of **GMP-regulated environments **, with exposure to audits, documentation review, validation protocols, and SOPs.

- Familiarity with deviation reporting, root cause analysis, and document control processes.

- Ability to follow established procedures and accurately execute formulations.

- Strong attention to detail and documentation accuracy.

- Effective communication skills and ability to collaborate cross-functionally.

- **Proactive, resourceful, and hands-on mindset ** with a “go-getter” attitude.

- Ability to think critically, take initiative, and step up in a dynamic environment.

**Preferred Qualifications (Nice-to-Have) **

- Team lead or supervisory experience in a manufacturing environment.

- Combination of **operational and quality experience **.

- Prior experience in IVD or regulated manufacturing settings.

**About Us: **

Founded in 2009, IntelliPro is a global leader in talent acquisition and HR solutions. Our commitment to delivering unparalleled service to clients, fostering employee growth, and building enduring partnerships sets us apart. We continue leading global talent solutions with a dynamic presence in over 160 countries, including the USA, China, Canada, Singapore, Japan, Philippines, UK, India, Netherlands, and the EU.

IntelliPro, a global leader connecting individuals with rewarding employment opportunities, is dedicated to understanding your career aspirations. As an Equal Opportunity Employer, IntelliPro values diversity and does not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, age, genetic information, disability, or any other legally protected group status. Moreover, our Inclusivity Commitment emphasizes embracing candidates of all abilities and ensures that our hiring and interview processes accommodate the needs of all applicants. Learn more about our commitment to diversity and inclusivity at https://intelliprogroup.com/.

**Compensation: **The pay offered to a successful candidate will be determined by various factors, including education, work experience, location, job responsibilities, certifications, and more. Additionally, IntelliPro provides a comprehensive benefits package, all subject to eligibility.

Formulation Chemist/Manufacturing/QA (GMP)

Industry: IT Services and IT Consulting
Company Size: 2-10 employees

FetchJobs.co

**About The Company**

WuXi AppTec is a leading global pharmaceutical, biotechnology, and medical device R&D service company dedicated to enabling the development of innovative medicines and healthcare products. With a commitment to scientific excellence and operational efficiency, WuXi AppTec offers comprehensive solutions across the entire drug development lifecycle, from discovery through manufacturing. The company operates state-of-the-art laboratories and manufacturing facilities worldwide, fostering a collaborative environment that promotes innovation, safety, and quality. WuXi AppTec’s mission is to accelerate the development of healthcare products that improve patients’ lives, making it an employer of choice for professionals seeking to contribute to impactful scientific advancements.

**About The Role**

Reporting directly to the QC Microbiology Lead, the QC Analyst plays a vital role in supporting microbiological testing and environmental monitoring activities essential for drug product manufacturing at WuXi AppTec’s Middletown, DE site. This position involves performing routine and non-routine microbiological assays, ensuring compliance with Good Manufacturing Practices (GMP), and maintaining thorough documentation to support product release, stability studies, and validation processes. The QC Analyst will work closely with cross-functional teams to ensure timely and accurate completion of laboratory tasks, uphold regulatory standards, and contribute to the overall quality assurance of pharmaceutical products. This role offers an excellent opportunity for professionals passionate about microbiology and quality control to contribute to innovative healthcare solutions in a dynamic, regulated environment.

**Qualifications**

- Associate or bachelor's degree in Microbiology, Biology, or a related scientific discipline.

- 1-3 years of quality control microbiology experience within a GMP-regulated pharmaceutical or biotechnology setting; internship or co-op experience will be considered.

- Proficiency in microbiological techniques and familiarity with laboratory instrumentation.

- Knowledge of GMP regulations, USP, ICH guidelines, and data integrity principles.

- Strong attention to detail, organizational skills, and the ability to work independently and as part of a team.

**Responsibilities**

- Perform microbiological testing on drug products, raw materials, packaging components, and utilities following approved methods and SOPs.

- Conduct environmental monitoring, bioburden, endotoxin, microbial limits, and microbial identification tests.

- Accurately document and report test results, ensuring compliance with data integrity principles (ALCOA+).

- Operate, calibrate, and maintain microbiology laboratory equipment in accordance with GMP standards.

- Support environmental monitoring programs and stability testing activities to ensure ongoing compliance and product quality.

- Assist in investigations of deviations, out-of-specification (OOS) results, and atypical findings, escalating issues as necessary.

- Prepare and review laboratory documentation, including testing records, validation protocols, and reports.

- Participate in internal and external audits by providing documentation and responding to inquiries.

- Maintain a safe and compliant laboratory environment by adhering to safety policies and procedures.

- Collaborate with cross-functional teams to support continuous improvement initiatives and operational excellence.

**Benefits**

WuXi AppTec offers a comprehensive benefits package designed to support the health, well-being, and professional growth of its employees. Benefits include competitive salary packages, health insurance plans, dental and vision coverage, retirement savings plans, paid time off, and holidays. Employees have access to ongoing training and development programs to enhance their skills and career progression. The company also promotes a collaborative and inclusive work environment, fostering innovation and teamwork. Additional perks may include wellness programs, employee assistance programs, and opportunities for internal mobility within the organization.

Equal Opportunity

WuXi AppTec is an equal opportunity employer. We are committed to creating a diverse and inclusive workplace where all employees are valued and respected. We do not discriminate against any individual based on race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other characteristic protected by applicable laws. All qualified applicants will receive consideration for employment without regard to these factors. We believe that diversity drives innovation and excellence, and we are dedicated to fostering a work environment that reflects these values.

QC Analyst

Find Analytical Chemist jobs with Savvy's AI Recruiter. Browse thousands of opportunities from top companies including remote positions. Our AI-powered system matches you with roles that fit your skills and experience.