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

Savvy Admin PROD

We are looking for an Occupational Therapist 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.

**Physicians & Advanced Practice Clinicians**

In this role you will need to be an expert in healthcare. We are interested in a wide range of expertise, so relevant backgrounds include:

Physicians of all specialties (e.g., Internists, Cardiologists, Oncologists), Physician Assistants, Nurse Practitioners, Certified Nurse-Midwives, Certified Registered Nurse Anesthetists, Clinical Nurse Specialists, Registered Nurses.

**Therapists**

Physical Therapists, Occupational Therapists, Speech-Language Pathologists, Respiratory Therapists, Athletic Trainers, Massage/Recreational Therapists.

**Diagnostic & Laboratory Professionals**

Radiologic Technologists, Sonographers, MRI & Nuclear Medicine Technologists, Medical Laboratory Scientists, Phlebotomists, Histology & Genetics Technicians.

**Public Health & Specialized Roles**

Dietitians/Nutritionists, Genetic Counselors, Epidemiologists, Public Health Nurses.

**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 $50-$60 USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex healthcare related problems and evaluate their outputs

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

- Ensure the medical accuracy of model performance

**Qualifications**

- Fluency in English (native or bilingual level)

- A current or in progress medical degree

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.

#medicine

Occupational Therapist

We are looking for a Speech Language Pathologist 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.

**Physicians & Advanced Practice Clinicians**

In this role you will need to be an expert in healthcare. We are interested in a wide range of expertise, so relevant backgrounds include:

Physicians of all specialties (e.g., Internists, Cardiologists, Oncologists), Physician Assistants, Nurse Practitioners, Certified Nurse-Midwives, Certified Registered Nurse Anesthetists, Clinical Nurse Specialists, Registered Nurses.

**Therapists**

Physical Therapists, Occupational Therapists, Speech-Language Pathologists, Respiratory Therapists, Athletic Trainers, Massage/Recreational Therapists.

**Diagnostic & Laboratory Professionals**

Radiologic Technologists, Sonographers, MRI & Nuclear Medicine Technologists, Medical Laboratory Scientists, Phlebotomists, Histology & Genetics Technicians.

**Public Health & Specialized Roles**

Dietitians/Nutritionists, Genetic Counselors, Epidemiologists, Public Health Nurses.

**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 $50-$60 USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex healthcare related problems and evaluate their outputs

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

- Ensure the medical accuracy of model performance

**Qualifications**

- Fluency in English (native or bilingual level)

- A current or in progress medical degree

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.

#medicine

Speech Language Pathologist

We are looking for a Physical Therapy Assistant 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.

**Physicians & Advanced Practice Clinicians**

In this role you will need to be an expert in healthcare. We are interested in a wide range of expertise, so relevant backgrounds include:

Physicians of all specialties (e.g., Internists, Cardiologists, Oncologists), Physician Assistants, Nurse Practitioners, Certified Nurse-Midwives, Certified Registered Nurse Anesthetists, Clinical Nurse Specialists, Registered Nurses.

**Therapists**

Physical Therapists, Occupational Therapists, Speech-Language Pathologists, Respiratory Therapists, Athletic Trainers, Massage/Recreational Therapists.

**Diagnostic & Laboratory Professionals**

Radiologic Technologists, Sonographers, MRI & Nuclear Medicine Technologists, Medical Laboratory Scientists, Phlebotomists, Histology & Genetics Technicians.

**Public Health & Specialized Roles**

Dietitians/Nutritionists, Genetic Counselors, Epidemiologists, Public Health Nurses.

**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 $50-$60 USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex healthcare related problems and evaluate their outputs

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

- Ensure the medical accuracy of model performance

**Qualifications**

- Fluency in English (native or bilingual level)

- A current or in progress medical degree

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.

#medicine

Physical Therapy Assistant

We are looking for a Healthcare Expert 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.

**Physicians & Advanced Practice Clinicians**

In this role you will need to be an expert in healthcare. We are interested in a wide range of expertise, so relevant backgrounds include:

Physicians of all specialties (e.g., Internists, Cardiologists, Oncologists), Physician Assistants, Nurse Practitioners, Certified Nurse-Midwives, Certified Registered Nurse Anesthetists, Clinical Nurse Specialists, Registered Nurses.

**Therapists**

Physical Therapists, Occupational Therapists, Speech-Language Pathologists, Respiratory Therapists, Athletic Trainers, Massage/Recreational Therapists.

**Diagnostic & Laboratory Professionals**

Radiologic Technologists, Sonographers, MRI & Nuclear Medicine Technologists, Medical Laboratory Scientists, Phlebotomists, Histology & Genetics Technicians.

**Public Health & Specialized Roles**

Dietitians/Nutritionists, Genetic Counselors, Epidemiologists, Public Health Nurses.

**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 $50-$60 USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex healthcare related problems and evaluate their outputs

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

- Ensure the medical accuracy of model performance

**Qualifications**

- Fluency in English (native or bilingual level)

- A current or in progress medical degree

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.

#medicine

Healthcare Expert

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

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

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

Merck

**Job Description**

**Job Description:**

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

**Education Minimum Requirement**

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

Or

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

Or

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

**Qualifications**

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

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

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

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

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

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

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

**Preferred Experience And Skills**

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

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

- undefined.

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

**Required Skills**

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

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

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

**Requirements**

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

EEOC Know Your Rights

EEOC GINA Supplement

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

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

**U.S. Hybrid Work Model**

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

The salary range for this role is

$117,000.00 - $184,200.00

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

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

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

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

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

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

**Search Firm Representatives Please Read Carefully**

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

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

1st - Day

**Valid Driving License**

No

**Hazardous Material(s)**

Yes

**Job Posting End Date**

04/25/2026

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

**Requisition ID: **R392202

Senior Scientist, Chemistry - Onsite

We are looking for a Clinical Specialist 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.

**Physicians & Advanced Practice Clinicians**

In this role you will need to be an expert in healthcare. We are interested in a wide range of expertise, so relevant backgrounds include:

Physicians of all specialties (e.g., Internists, Cardiologists, Oncologists), Physician Assistants, Nurse Practitioners, Certified Nurse-Midwives, Certified Registered Nurse Anesthetists, Clinical Nurse Specialists, Registered Nurses.

**Therapists**

Physical Therapists, Occupational Therapists, Speech-Language Pathologists, Respiratory Therapists, Athletic Trainers, Massage/Recreational Therapists.

**Diagnostic & Laboratory Professionals**

Radiologic Technologists, Sonographers, MRI & Nuclear Medicine Technologists, Medical Laboratory Scientists, Phlebotomists, Histology & Genetics Technicians.

**Public Health & Specialized Roles**

Dietitians/Nutritionists, Genetic Counselors, Epidemiologists, Public Health Nurses.

**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 $50-$60 USD per hour, with bonuses on high-quality and high-volume work

**Responsibilities**

- Give AI chatbots diverse and complex healthcare related problems and evaluate their outputs

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

- Ensure the medical accuracy of model performance

**Qualifications**

- Fluency in English (native or bilingual level)

- A current or in progress medical degree

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.

#medicine

Clinical Specialist

At Personalis, we are transforming the active management of cancer through breakthrough personalized testing. We aim to drive a new paradigm for cancer management, guiding care from biopsy through the life of the patient. Our highly sensitive assays combine tumor-and-normal profiling with proprietary algorithms to deliver advanced insights even as cancer evolves over time. Our products are designed to detect minimal residual disease (MRD) and recurrence at the earliest timepoints, enable selection of targeted therapies based on ultra-comprehensive genomic profiling, and enhance biomarker strategy for drug development. Personalis is based in Fremont, California.

Industry: Biotechnology Research
Company Size: 201-500 employees

Personalis, Inc.

Personalis, Inc. is a leader in advanced genomics for precision oncology. NeXT Personal is an ultra-sensitive, tumor-informed, WGS-based liquid biopsy assay designed to detect minimal residual disease (MRD) and cancer recurrence. It leverages whole-genome sequencing of a patient's tumor and matched normal samples to create personalized panel of up to 1,800 somatic variants, enabling the detection of circulating tumor DNA (ctDNA) at very low levels (down to ~1-3 PPM) in blood samples. To enable cancer and population sequencing, Personalis' Clinical Laboratory was built with a focus on clinical accuracy, quality, big data, scale, and efficiency.

**Days Onsite: Monday & Tuesday**

**Summary:**

The Senior Bioinformatics Scientist will work with a world-class, dynamic team of bioinformatics scientists, software engineers, and laboratory scientists, developing, testing, and applying cutting-edge cell-free and solid tumor cancer genomics products. Further, the Senior Bioinformatics Scientist will work closely with our clinical evidence generation teams, applying our cell-free technology solutions to large cancer patient cohorts and profiling patient response to therapy with our cfDNA platforms. This position will directly contribute to a new generation of genomics-based precision-medicine products for profiling MRD, ctDNA dynamics, and patient response to treatment. Our products are used by pharma, biotech, hospitals, and clinicians for managing patient treatment and therapeutic selection.

**Responsibilities:**

- Design and develop novel cell-free technologies and products

- Collaborate closely with laboratory scientists to design experiments to develop and evaluate novel applications for cell-free DNA assays

- Draw on deep experience with genomics and statistics to model and improve performance of cell-free assays and features

- Synthesize large datasets to develop and evaluate new biological and technological hypotheses

- Partner with the clinical evidence generation team to ensure the applicability and evaluate the performance of novel assays or feature improvements

- Maintain a strong working knowledge of literature covering technological developments in the cell-free DNA and liquid biopsy space

- Publish results and present at conferences in exciting areas, including cell-free DNA and cancer genomics

**Requirements:**

- Advanced degree (Ph.D.) in bioinformatics, genomics, or a related field

- Extensive experience with cancer genomics

- Extensive experience with somatic mutational detection and filtering

- Experience with cancer liquid biopsy analysis

- Proficiency in the application of statistical methods to genomic applications

- Proficiency with at least one common programming language (e.g., Python, R)

- A track record of designing and implementing experimental approaches to confirm and elaborate upon findings from complex projects

- Experience publishing and presenting scientific results

The hiring range for this position is $155,000 to $190,000 per year, which may factor in various geographic regions. The base pay actually offered will take into account internal equity and also may vary depending on the candidate’s geographic region, job-related knowledge, skills, and experience among other factors. Our full-time regular positions also include an annual performance-based bonus (or a sales incentive plan) and long-term incentive units (equity) provided as part of our compensation package, in addition to a full range of medical, financial, and/or other benefits, dependent on the level and position offered.

Personalis is an equal opportunity employer and is committed to the full inclusion of all individuals. As part of this commitment, Personalis will ensure that persons with disabilities are provided with reasonable accommodations. If you need an accommodation to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please let your recruiter know, if/when they contacts you.

**Protecting Our Candidates: ** At Personalis, we value your security. Please note that all official correspondence from our team will come exclusively from **@ ****personalis.com ** email addresses. We will never ask for personal financial information or conduct interviews over text or chat platforms. If you receive a suspicious request, it is likely a scam. We are committed to a safe recruitment experience and actively work with authorities to investigate and prosecute cyber crimes targeting our community.

~~Personalis offers a competitive compensation package and benefits including medical, dental, vision, 401(k) match, ESPP, tuition reimbursement, sick/vacation time, commuter benefits/ EV charging stations, onsite gym, and wellness benefits. (For US only, benefits in other countries may vary.) ~~

Sr. Bioinformatics Scientist – Novel Cell Free DNA Applications

Come for a job. Stay for a career. Make a difference for a lifetime!

GROW your career! Looking for interesting and diverse career opportunities?  Look no further!  Explore the many unique and fascinating jobs found across the Commonwealth of Kentucky.  

LEARN with us!  The Commonwealth of Kentucky offers our employees on-the-job training and online professional development courses. With thousands of unique positions available throughout the Commonwealth, you can increase your knowledge on the job -- and set your career goals for the future.  

LEAD with us!   We are a community of doers, thinkers, learners, leaders, and achievers.  We can help you  find your perfect job match and then excel in that role.  We have programs and tools to help you grow in your position and become a leader as the best version of yourself! 

SERVE with us!  Careers in public service are diverse, interesting and rewarding.  They allow you to truly make a difference in the communities that you serve.  If you have a passion around serving your community while you grow your skills and your career, join the many employees across the Commonwealth who are finding perfect work opportunities and getting the satisfaction of touching lives and making a lasting impact.

Achieve your professional goals while working for Commonwealth’s largest employer. Whether this is your first job or you’re transitioning from the military or another career, we offer a diverse opportunity for all educational and experience levels in full-time, part-time, temporary, or seasonal capacities. Employees can work in a civil service, non-civil service, appointed, or elected position. Come grow, learn, lead and serve with us!

For employment opportunities with the Commonwealth of Kentucky, visit careers.ky.gov.

Industry: Government Administration
Company Size: 10,001+ employees

Commonwealth of Kentucky

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4/12/2026 (8:00 PM EDT)

26-01633

Public Health Lab Scientist-in-Training

Pay Grade 12

Salary

$35,712.48 - $53,568.48 Annually

Employment Type

EXECUTIVE BRANCH | FULL TIME | ELIGIBLE FOR OVERTIME PAY | 18A | 37.5 HR/WK

Click here for more details on state employment.

Hiring Agency

Cabinet for Health & Family Services | Department for Public Health

Location

100 Sower Boulevard

Frankfort, KY 40601 USA

**Description**

The Department for Public Health, Division of Laboratory Services, Newborn Screening Branch is dedicated to improving the health and safety of Kentucky newborns through prevention, promotion, and protection. This Laboratory Scientist-In-Training position allows the individual to learn to perform critical, life-saving testing of inborn errors of metabolism. The Branch works with birthing facilities across the state to ensure mandated testing services are provided to all Kentucky-born newborns. The Division strives to allow individuals to enhance their laboratory skills through advanced training in state-of-the-art technologies and provides opportunities for advancement through the laboratory career ladder.

The Metabolic Chemistry Section of the Molecular and Clinical Chemistry Branch is responsible for testing approximately 50,000 babies born in Kentucky each year. This testing allows for treatment to begin as soon as possible in the affected infants’ lives, thereby eliminating or reducing the devastating effects of the screened disorders, which could include permanent physical and/or mental disability or death. This position is in the office and does not offer a hybrid schedule. The work schedule is Tuesday- Saturday, 8-4:30 PM.

The Division is seeking a Laboratory Scientist-In-Training to learn to perform tandem mass spectrometry, real- time polymerase chain reaction, and DNA mutation analyses for the KY Newborn Screening Program. This individual will work with our state partners, such as the Division of Maternal and Child Health, and our federal partners, including the Centers for Disease Control and Prevention (CDC). The candidate for this position needs to be a fast learner, enthusiastic, motivated to do an excellent job, eager to improve systems, and willing to keep the team informed of issues. The successful candidate must be professional, polite, detail-oriented, and familiar with the Health Insurance Portability and Accountability Act (HIPAA).

Responsibilities and Duties include but are not limited to the following:

- Gain and maintain knowledge concerning testing for inborn errors of metabolism, in which state-of-the-art technology is used to detect genetic disorders in newborns before they exhibit symptoms.

- Learn to perform Tandem mass spectrometry.

-  Learn to perform testing and analysis, including automated molecular testing by polymerase chain reaction (PCR).

-  Learn to perform DNA mutation analysis.

-  Learn to perform automated immunoassays for Newborn Screening.

- Perform testing for after hours, holiday and weekend coverage for public health events and incidents

**Qualifications And Skills**

- Ability and desire to learn quickly.

-  Understanding of application and use of immunoassays and other routine scientific assays.

-  Understanding of Microsoft Word and Excel,

-  Computer literacy.

-  Strong written and verbal communication.

-  Ability to work with others.

- Adhere to confidentiality requirements (HIPAA).

-  Self-starter with the initiative to problem-solve scientific and instrument issues.

The Cabinet for Health and Family Services (CHFS) participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in U.S. CHFS will only use E-Verify once you have accepted a job offer and completed the Form I-9. For more information on E-Verify, or if you believe that CHFS has violated its E-Verify responsibilities, please contact Department of Homeland Security (DHS) at 888-897-7781 or https://www.e-verify.gov/ .

**Minimum Requirements**

**EDUCATION: ** Graduate of a college or university with a bachelor's degree in medical laboratory science, biology, chemistry, microbiology, medical technology, zoology, forensics science, animal science, biochemistry, molecular biology, cellular biology, health science, biomedical engineering, environmental biology, ecology, pre-med studies, agricultural engineering, bacteriology, biochemistry, physics, biophysics, dairy science, genetics, pathology, veterinary medicine, histology or a related field.

**EXPERIENCE, TRAINING, OR SKILLS: ** NONE

**Substitute EDUCATION for EXPERIENCE: ** NONE

**Substitute EXPERIENCE for EDUCATION: ** NONE

**SPECIAL REQUIREMENTS (AGE, LICENSURE, REGULATION, ETC.): ** NONE

Working Conditions

Work is typically performed in a laboratory setting. May be exposed to potential hazards related to laboratory conditions and supplies which may require the following of safety precautions.

Probationary Period

This job has an initial and promotional probationary period of 6 months, except as provided in KRS 18A.111.

If you have questions about this advertisement, please contact Amy Smith at AmyC.Smith@ky.gov or 502-782-7747.

An Equal Opportunity Employer M/F/D

Public Health Lab Scientist-in-Training

Advertisement Closes

4/18/2026 (8:00 PM EDT)

26-01718

Public Health Laboratory Scientist III

Pay Grade 15

Salary

$47,531.28 - $71,298.00 Annually

Employment Type

EXECUTIVE BRANCH | FULL TIME | ELIGIBLE FOR OVERTIME PAY | 18A | 37.5 HR/WK

Click here for more details on state employment.

Hiring Agency

Cabinet for Health & Family Services | Department for Public Health

Location

100 Sower Boulevard

Suite 204

Frankfort, KY 40601 USA

**Description**

The Department for Public Health, Division of Laboratory Services, Microbiology Branch, is dedicated to improving the health and safety of Kentucky citizens through prevention, promotion, and protection. The Public Health Laboratory Scientist III position provides the individual with the opportunity to perform critical, life-saving testing for various viral and bacterial diseases. The Branch works with submitting facilities across the state to ensure requested and mandated testing services are provided to all citizens living in the Commonwealth.

The Division strives to allow individuals to enhance their laboratory skills through advanced trainings in state–of-the-art technologies. The Virology Section of the Microbiology Branch is responsible for providing testing for the approximately 5,000 specimens received each month. This testing allows for treatment to begin as soon as possible in the affected individuals' lives, thereby eliminating or reducing the effects of the infections, which could include permanent physical and mental disability or death. We offer generous vacation and sick leave, health insurance, professional development and training, and participation in our state retirement plan.

The Division is seeking a Public Health Laboratory Scientist III to perform enzyme-linked immunosorbent assays, real-time polymerase chain reaction analysis, and animal necropsies for the submitting facilities in Kentucky. This individual will work with our state partners, such as the Division of Epidemiology, and our federal partners, including the Centers for Disease Control and Prevention (CDC). The candidate for this position needs to be a fast learner, enthusiastic, motivated to do an excellent job, eager to improve systems, and willing to keep the team informed of issues. The successful candidate must be professional, polite, detail-oriented, and familiar with the Health Insurance Portability and Accountability Act (HIPAA).

Responsibilities and Duties include, but are not limited to the following:

- Gains and maintains knowledge concerning testing for infectious viral diseases and the associated pathogens

-  Performs routine and complex testing and analysis, including molecular testing by polymerase chain reaction (PCR)

-  Performs Enzyme Linked Immunosorbent Assays (EIA)

-  Performs animal necropsies on rabies suspect specimens

-  Performs automated immunoassays for viral or bacterial diagnoses

-  Performs testing for after-hours, holiday, and weekend coverage for public health events and incidents

-  Compiles monthly reports and keeps them up to date

-  Collects data and monitors quality assurance metrics

-  Ensures compliance with and enforcement of accreditation program standards

-  Collects and reports data to be used for departmental research that improves public health practices

**Qualifications And Skills**

- Ability and desire to learn quickly

-  Thorough knowledge of polymerase chain reaction testing

-  Understanding of application and use of immunoassays

-  Understanding of Microsoft Word, Excel, PowerPoint, Adobe, and other similar products

-  Computer literacy

-  Strong written and verbal communication

-  Ability to work with others: motivates, delegates, and mediates

-  Adhere to confidentiality requirements (HIPAA)

The Cabinet for Health and Family Services (CHFS) participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in U.S. CHFS will only use E-Verify once you have accepted a job offer and completed the Form I-9. For more information on E-Verify, or if you believe that CHFS has violated its E-Verify responsibilities, please contact Department of Homeland Security (DHS) at 888-897-7781 or https://www.e-verify.gov/ .

**Minimum Requirements**

**EDUCATION: ** Graduate of a college or university with a bachelor's degree in medical laboratory science, biology, chemistry, microbiology, medical technology, zoology, forensics science, animal science, biochemistry, molecular biology, cellular biology, health science, biomedical engineering, environmental biology, ecology, pre-med studies, agricultural engineering, bacteriology, biochemistry, physics, biophysics, dairy science, genetics, pathology, veterinary medicine, histology or a related field.

**EXPERIENCE, TRAINING, OR SKILLS: ** Three years of professional laboratory work conducting laboratory testing.

**Substitute EDUCATION for EXPERIENCE: ** Certification as a Medical Technologist or a Medical Laboratory Scientist by the American Society for Clinical Pathology will substitute for one year of experience OR master's degree in medical laboratory science, medical technology, chemistry, any biological, physical, or agricultural science, including microbiology, virology, immunology, bacteriology, histology, molecular microbiology or a related field will substitute for one year of experience.

**Substitute EXPERIENCE for EDUCATION: ** NONE

**SPECIAL REQUIREMENTS (AGE, LICENSURE, REGULATION, ETC.): ** NONE

Working Conditions

Work is typically performed in a laboratory setting. May be exposed to potential hazards related to laboratory conditions and supplies which may require the following of safety precautions.

Probationary Period

This job has an initial and promotional probationary period of 6 months, except as provided in KRS 18A.111.

If you have questions about this advertisement, please contact Teresa Fields at Teresa.Fields@ky.gov or 502-782-7718.

An Equal Opportunity Employer M/F/D

Public Health Laboratory Scientist III

**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

**Job Description**

**Job Location:**

West Point, PA

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

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

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

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

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

- Manage data integrity through automated processes.

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

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

**Education Minimum Requirements**

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

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

**Required Experience And Skills**

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

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

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

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

- Strong verbal and written communication skills

- Experience in good documentation practices.

- Self-starter with ability to work independently.

- Ability to follow procedures and thoroughly document experiments.

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

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

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

**Preferred Experience And Skills**

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

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

**Required Skills**

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

**Preferred Skills**

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

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

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

**Requirements**

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

EEOC Know Your Rights

EEOC GINA Supplement

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

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

**U.S. Hybrid Work Model**

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

The salary range for this role is

$87,300.00 - $137,400.00

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

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

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

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

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

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

**Search Firm Representatives Please Read Carefully**

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

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

Yes

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

N/A

**Job Posting End Date**

04/24/2026

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

**Requisition ID: **R392976

Scientist, Pharmacokinetics

**Job Description**

**Job Location:**

West Point, PA

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

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

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

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

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

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

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

**Education Minimum Requirements**

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

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

- undefined

**Required Experience And Skills**

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

- Good verbal and written communication skills

- Ability to follow procedures and thoroughly document experiments.

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

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

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

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

**Preferred Experience And Skills**

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

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

**Required Skills**

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

**Preferred Skills**

Current Employees apply HERE

Current Contingent Workers apply HERE

**US And Puerto Rico Residents Only**

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

**Requirements**

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

EEOC Know Your Rights

EEOC GINA Supplement

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

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

**U.S. Hybrid Work Model**

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

The salary range for this role is

$87,300.00 - $137,400.00

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

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

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

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

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

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

**Search Firm Representatives Please Read Carefully**

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

**Employee Status**

Regular

**Relocation:**

Domestic

**VISA Sponsorship**

No

**Travel Requirements**

No Travel Required

**Flexible Work Arrangements**

Not Applicable

**Shift**

Not Indicated

**Valid Driving License**

No

**Hazardous Material(s)**

N/A

**Job Posting End Date**

04/23/2026

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

**Requisition ID: **R393012

Orum Therapeutics (KRX: 475830) is a public biotechnology company developing TPD2®, a novel class of targeted protein degradation therapeutics. Also known as degrader-antibody conjugates (DACs), these therapeutics combine the precision of antibodies with Orum's novel degrader payloads to break down disease-causing proteins inside specific cells.

By enabling the selective degradation of previously “undruggable” targets, Orum is working to improve the effectiveness, safety, and reach of targeted protein degradation. The company’s lead programs target GSPT1, and it is also advancing next-generation payloads to expand the potential of its DAC pipeline.
In parallel, Orum is developing proprietary linker technologies to increase the flexibility and precision of future DAC programs.

With headquarters in Daejeon, South Korea, and Lexington, Massachusetts, U.S., Orum is globally positioned to deliver first-in-class cancer therapies for patients with hard-to-treat diseases. For more information, visit www.orumrx.com.

Industry: Biotechnology Research
Company Size: 51-200 employees

Orum Therapeutics

Orum Therapeutics is seeking a highly motivated and accomplished scientist to lead the Bioanalytical (BioA) and PK/PD function. This role is designed for a technical expert who thrives at the intersection of large and small molecule analysis, specifically focused on the complex characterization of Antibody-Drug Conjugates (ADCs). As a key scientific lead, you will orchestrate the bioanalytical lifecycle — from internal method innovation to global CRO oversight — ensuring high-quality data generation in a GLP/GCP environment. Beyond assay management, you will serve as a strategic partner in project teams, leveraging pharmacokinetic modeling to translate data into actionable insights that drive candidate selection and program progression.

Principal Duties and Responsibilities

- Design and execute integrated Bioanalytical and PK/PD strategies for ADC programs, utilizing the three-analyte quantification approach (Total Ab, Conjugated, and Free Payload) from lead optimization to IND filing.

- Oversee in vitro and in vivo ADME studies, including payload metabolism, drug-drug interactions (DDI), and transporter assays, to define the metabolic fate of the ADC and the released payload.

- Provide high-level technical oversight for hybrid bioanalytical workflows, specifically bridging LBA and LC-MS/MS platforms to ensure robust quantification of complex modalities.

- Lead CRO selection and management, serving as the primary point of contact for method transfer, development, validation, and troubleshooting of proprietary assays under aggressive timelines.

- Review and approve SOPs, validation reports, and bioanalytical study plans in alignment with GLP/GCP standards and current FDA guidance.

- Act as the BioA/PK subject matter expert (SME) within multidisciplinary project teams, collaborating with Research & Development and Clinical teams to drive program milestones.

- Drive continuous improvement by evaluating emerging technologies to enhance the throughput and quality of ADC characterization.

- Execute an integrated role that bridges high-level scientific leadership and direct lab-based contributions, ensuring seamless translation from internal innovation to external CRO execution.

- Serve as the lead author for BioA and PK sections of regulatory submissions (IND/IB), ensuring full compliance with GLP/GCP and current FDA/EMA bioanalytical guidance.

**Skills, Abilities & Competencies**

- Extensive experience in pharmacokinetic (PK) and biodistribution studies of Antibody-Drug Conjugates (ADCs), including application of advanced bioanalytical methods such as LC-MS/MS for small-molecule quantitation and MSD-based ligand-binding assays (LBAs).

- Proven track record in developing, validating, and implementing bioanalytical assays for ADC modalities, including total antibody, free and conjugated payload, and anti-drug antibodies (ADA) assays, in support of preclinical and clinical PK studies.

- In-depth understanding of ADME principles and drug discovery/development workflows, including screening strategies from early feasibility through candidate nomination.

- Experience in non-compartmental analysis of PK data, with hands-on experience in PK/PD modeling and simulation, population PK analysis, and meta-analysis is a plus.

- Working knowledge of GLP and GCP regulations and their application within bioanalytical and clinical study environments.

- Demonstrated ability to operate independently in fast-paced biotech settings while effectively collaborating within cross-functional, global teams.

- Excellent communication, organizational, and time-management skills, with the ability to manage multiple priorities and deliver high-quality results.

- Strong work ethic with a high degree of accountability, initiative, and ability to work with minimal supervision.

Education

Ph.D. or equivalent degree in Analytical Chemistry or a related field with a minimum of 5 years' experience. Level will be commensurate with experience and accomplishments.

- U.S. citizens and those authorized to work in the U.S. (green card) are encouraged to apply. We are unable to sponsor/transfer at this time.

- Candidate must be able to pass a background investigation.

- Unable to work with 3rd party candidates or agencies.

~~To perform this job successfully, an individual must be able to perform each essential duty satisfactorily within the context of the representative work environment and physical demands described above. Likewise, qualifications listed are representative of the knowledge, skills, and abilities required to perform the position’s essential functions. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.~~

~~Orum Therapeutics is an Equal Opportunity Employer (EOE). ~~

Bioanalytical Scientist

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

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

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

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

Astrix

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

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

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

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

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

**Pay Rates**

(1–3 years): Up to $36/hr

(3–5 years): Up to $40/hr

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

**Key Responsibilities**

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

- Conduct analytical testing and review data for accuracy and completeness

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

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

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

- Support method validation, calibration, and equipment maintenance

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

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

**Qualifications**

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

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

- Hands-on experience with HPLC (required)

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

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

- Strong understanding of GMP and documentation practices

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

INDBH

Quality Control Scientist

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

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

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

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

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

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

Planet Pharma

Pay 30-40/h depending on experience

**Purpose**

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

**Essential Job Responsibilities**

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

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

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

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

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

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

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

- Support and mentor junior team members

- Collaborate with other network sites to share best practices

- Other duties as required

**Quantitative Dimensions**

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

**Organizational Context**

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

**Qualifications**

Required:

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

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

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

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

- Ensures inspection, testing and release timelines are met.

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

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

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

- Successfully performs work independently with minimal instructions

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

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

- Highly self-motivated and goal oriented

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

**Preferred:**

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

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

- Experience in method validation/qualification/verification/transfer

**Working Conditions:**

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

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

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