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Associate Principal Scientist, Analytical R&D (GxP Supervisor 2nd Shift)

Merck

Rahway, NJFull-time$142–224K/yrSeen 1w agoSeen in employer's feed 1 day ago

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At a glance

Compensation
$142–224K/yr
Location
Rahway, NJ
Schedule
Full-time
Work Authorization
Visa required • Visa sponsorship

Olive lists jobs from US employers, including remote roles you can work from the United States.

Job overview

The Associate Principal Scientist will supervise a team supporting GMP analytical activities for Merck’s non-sterile clinical portfolio at its Rahway site during second-shift operations. The role combines scientific and operational oversight with hands-on analytical laboratory support for drug substance and drug product. It also supports clinical manufacturing through analytical testing, compliance oversight, data review, process improvement, and collaboration with internal stakeholders and partners.

Skills & qualifications

RequiredNice to have

Skills

Scientific CommunicationCreativityInterpersonal SkillsTeam LeadershipCollaborationAnalytical Method DevelopmentAnalytical TestingAssay DevelopmentBiological Assay DevelopmentCell-Based AssaysChromatographic TechniquesCleaning ValidationsDrug DevelopmentHigh Resolution Mass SpectrometryLiquid Chromatography-Mass SpectrometryPharmaceutical Process DevelopmentProcess Analytical TechnologyProtein AnalysisRegulatory Compliance AuditsGMP Analytical Lab ManagementLab InvestigationsCompliance Audits

Qualifications

BS or MS in Chemistry or Related SciencePhD in Chemistry or Related ScienceBS/MS+7 or PhD+3 YearsGMP Analytical Lab Management ExperienceLab Investigations and Deviations Experience

Benefits

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Match
Paid Time Off

Full job description

Job Description

Role Summary:

Join us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

The Associate Principal Scientist will serve as the scientific and operational supervisor for a team of specialists and scientists in Rahway supporting various GMP analytical activities including cleaning verification, method validation, solvent release, and in-process testing for drug substance and drug product across the entirety of our non-sterile clinical portfolio during 2nd shift operations at the Rahway site. The role will also require hands-on analytical lab support to enable the pipeline.

Primary Responsibilities:

  • Serve as a scientific and operational supervisor for a team of specialists and scientists supporting cleaning verification, solvent release, and in-process testing for drug substance and drug product during 2nd shift operations.

  • Support execution of Good Manufacturing Practices (GMP) analytical activities such cleaning verification, method validation and in-process testing.

  • Document the execution, procedure, results, and conclusions of experiments in a detailed and organized manner following ALCOA+ principles.

  • Ensure on time, right first-time analytical testing to enable clinical manufacture of drug substance and drug product.

  • Provide technical and compliance oversight for lab investigations and deviations and to troubleshoot in the lab as necessary.

  • Review and approval of GMP data, analytical reports, and SOPs.

  • Ensure operational excellence and drive process improvements.

  • Work collaboratively with internal stakeholders and partners such as Global Development Quality and Pharmaceutical Operations.

  • Support internal and external compliance audit activities.

Qualifications:

Education Minimum Requirements:

  • BS or MS in chemistry or related science with at least 7 years of industry experience with pharmaceutical drug substance and/or product development.

  • Ph.D. in chemistry or related science with at least 3 years of industry experience with pharmaceutical drug substance and/or product development.

Required Experience and Skills:

  • Excellent scientific communication skills.

  • Demonstrated creativity.

  • Effective interpersonal and collaborative skills.

  • Demonstrated ability to lead teams to deliver high-quality results against firm deadlines.

  • Ability to partner in a team environment with cross-functional interactions to drive results.

Preferred Experience and Skills

  • Prior experience managing a GMP analytical lab that supports cleaning verification.

  • IPC, and solvent release.

  • Prior experience with lab investigations/deviations and compliance audits is a plus.

#AR&D

Required Skills:

Analytical Method Development, Analytical Testing, Assay Development, Biological Assay Development, Cell-Based Assays, Chromatographic Techniques, Cleaning Validations, Drug Development, High Resolution Mass Spectrometry (HRMS), Liquid Chromatography-Mass Spectrometry (LC-MS), Pharmaceutical Process Development, Process Analytical Technology (PAT), Protein Analysis, Regulatory Compliance Audits

Preferred Skills:

Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld)

Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)

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 (https://survey.sogosurvey.com/r/aCdfqL) if you need an accommodation during the application or hiring process.

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 (https://www.eeoc.gov/sites/default/files/2022-10/22-088\_EEOC\_KnowYourRights\_10\_20.pdf)

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 (https://www.msdprivacy.com/us/en/CCPA-notice/)

The primary location for this posting is:

USA - New Jersey - Rahway

Where required by law, the compensation range for this role is provided below.

The salary range for the primary location of this role is:

$142,400.00 - $224,100.00

This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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 .

Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.

Additional location(s) Compensation Information:

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:

10%

Flexible Work Arrangements:

Not Applicable

Shift:

2nd - Evening

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

11/20/2026

*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: R423267

How this job compares

Set against the 1,432 open Research and Development jobs on Olive Jobs, counted November 6, 2026.

Pay
  • This posting$142–224K/yr
  • New Jersey median$113–153K/yr54 salary ranges
  • US median$118–171K/yr754 salary ranges

This range's midpoint, $183K, is 38% above the New Jersey median midpoint ($133K) — in the middle half of Research and Development salary ranges in New Jersey.

Openings
Olive Jobs lists 72 open Research and Development jobs in New Jersey and 1,432 across the US. 3% of them nationwide are listed as remote or flexible.
Hiring the most in New Jersey
Experience
This posting asks for at least 3 years of experience; Research and Development postings that state a minimum ask for 5 years at the median (949 postings).
Education
756 of the 1,432 open Research and Development jobs (53%) ask for a bachelor's degree or higher.

Counted across the open, public US postings on Olive Jobs on November 6, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.

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