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Cogent Biosciences

Senior Manager, Quality Control GMP

Cogent Biosciences · Remote, United States

Posted about 3 months ago · $155,000 - 185,000 · Previously reposted

or apply directly on Cogent Biosciences's site. We never take the application ourselves.

Is this posting real?

This role has been open
81 days
Cogent Biosciences's roles stay open a median of 43 days
Reposted
Yes
taken down and listed again at least once
Salary listed
Yes
92% of Cogent Biosciences's roles list one
Ghost-job risk at Cogent Biosciences
high
12 stale, 1 reposted of 25 open
Hiring momentum
32 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-10-24

Measured from postings appearing on and disappearing from Cogent Biosciences's own greenhouse board since 2026-08-03. Full hiring picture for Cogent Biosciences.

About this role

The Senior Manager, Quality Control GMP at Cogent Biosciences will lead Quality Control activities for clinical and commercial manufacturing, ensuring compliance with GMP standards. This role involves method lifecycle management, supporting release and stability testing, and collaborating with various teams to maintain robust QC operations. The successful candidate will also mentor junior staff and contribute to continuous improvement initiatives within the QC processes.

Our read on this posting4.8out of 5
benefits
5/5
freshness
5/5
career value
4/5
role clarity
5/5
pay transparency
5/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Cogent Biosciences as an employer.

What you need

  • Ph.D. in Chemistry, Pharmaceutical Sciences, or a related discipline, or M.S./B.S. with substantial relevant industry experience
  • 5-8 years of experience with QC testing and GMP compliance supporting clinical and/or commercial stage programs
  • Strong expertise in analytical techniques relevant to small-molecule pharmaceuticals (e.g., HPLC/UPLC, GC, dissolution, spectroscopic methods, and wet chemistry)
  • Deep understanding of method validation, transfer, and lifecycle management in a regulated environment
  • Demonstrated experience supporting or leading deviation investigations (OOS/OOT) and CAPA processes
  • Working knowledge of global regulatory requirements, including FDA, EMA, ICH guidelines, and compendial standards (USP, EP)

What you get

  • Competitive salary
  • Target bonus of 15%
  • 100% coverage of medical, dental, and vision premiums for employees and their families
  • Funding up to 75% of in-network deductibles
  • 401(k) match with immediate vesting
  • Generous paid time off

Worth weighing

  • Remote position may limit in-person collaboration opportunities
  • No specific mention of the company's technology stack or tools used in QC processes

Summarised from Cogent Biosciences's posting. Read the full original.

Listed by Cogent Biosciences on their greenhouse job board, last confirmed open on 2026-10-24. PitchMeAI is not the employer.

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