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KH

Senior GMP Quality Manager

Katalyst Healthcares & Life Sciences
Location not stated
Remote
Manager or above
3 weeks ago
  • CMOS
  • GMP

Not enough detail in this posting to match

Key Responsibilities
  • Lead sponsor-side QA oversight of CMOs across pre-clinical, clinical, and commercial manufacturing — drug substance, drug product, and final product
  • Own quality oversight for commercial-stage drug substance activities, including process validation (PPQ) and disposition
  • Serve as QA SME on deviations, CAPAs, change controls, and documentation revisions
  • Review and approve CMO documentation, batch records, and test data; perform product dispositions
  • Support quality review of regulatory submissions (IND/IMPD, NDA) and participate in inspection readiness
  • Represent QA cross-functionally with CMC, Supply Chain, and Analytical Development
  • Maintain quality metrics and periodically revise GMP SOPs
Qualifications
  • Bachelor's degree in a scientific or technical discipline
  • 8+ years GMP Quality experience in pharma, including late-stage drug product development and validation
  • Sponsor-side CMO oversight experience — clinical-stage across DS/DP/FP, or commercial-stage specifically on drug substance
  • Experience with process validation (PPQ) and late-stage/commercial regulatory submissions
  • Inspection readiness experience (domestic and/or ex-US) preferred

Senior GMP Quality Manager · Katalyst Healthcares & Life Sciences

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