PitchMeAI Jobs
Revolution Medicines

Senior Manager, Quality Validation

Revolution Medicines · Redwood City, California, United States

Posted about a month ago

or apply directly on Revolution Medicines's site. We never take the application ourselves.

Is this posting real?

This role has been open
30 days
Revolution Medicines's roles stay open a median of 43 days
Reposted
No
Salary listed
No
0% of Revolution Medicines's roles list one
Ghost-job risk at Revolution Medicines
low
0 stale, 6 reposted of 264 open
Hiring momentum
449 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-09-17

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

About this role

The Senior Manager, Quality Validation at Revolution Medicines will oversee quality assurance for validation activities in commercial manufacturing, focusing on Process Performance Qualification (PPQ) and Continued Process Verification (CPV). This role involves collaborating with internal and external stakeholders to ensure compliance with regulatory requirements, managing validation lifecycle activities, and providing QA support across GMP operations. The position requires strong leadership and communication skills to build effective relationships and address quality-related challenges.

Our read on this posting3.2out of 5
benefits
3/5
freshness
4/5
career value
4/5
role clarity
5/5
pay transparency
0/5

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 Revolution Medicines as an employer.

What you need

  • Bachelor's degree in a scientific, engineering or technical discipline
  • Minimum of 8 years of experience in the pharmaceutical industry with GMP Quality and commercial manufacturing operations
  • Experience providing QA oversight of validation lifecycle activities, particularly PPQ and CPV
  • Strong knowledge of process validation lifecycle principles and applicable U.S. and global GMP regulations
  • Experience supporting commercial readiness, inspection readiness, and regulatory inspections
  • Ability to critically evaluate complex technical and compliance issues and make sound, risk-based Quality decisions

Nice to have

  • Experience supporting validation and lifecycle management of commercial pharmaceutical products across multiple CMOs
  • Experience with late-stage development, commercial launch, technology transfer, and post-approval lifecycle management activities
  • Experience with statistical trending and evaluation of CPV data
  • Experience working with oral solid dosage forms and associated manufacturing and packaging operations

What you get

  • Base pay salary range of $164,000 — $205,000 USD
  • Competitive cash compensation
  • Robust equity awards
  • Strong benefits
  • Significant learning and development opportunities

Worth weighing

  • No specific mention of remote work flexibility despite hybrid label
  • Salary range provided but may vary based on local market and individual factors
  • Focus on compliance and quality oversight may limit exposure to innovative technical challenges

Summarised from Revolution Medicines's posting. Read the full original.

Listed by Revolution Medicines on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.

More roles at Revolution Medicines

All 264 open roles at Revolution Medicines →