GMP Validation Writer: SOPs, Protocols & Compliance
Listed on 2026-10-06
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Pharmaceutical
Healthcare Compliance -
Healthcare
Healthcare Compliance, Medical Science
Sentry Bio Pharma Services, Inc. is seeking a detail-oriented Validation Technical Writer to join our Validation team in Indianapolis, IN. The role focuses on ensuring accuracy, clarity, and regulatory compliance of GMP documentation for systems and facilities.
You will author validation reports (IQ/OQ/PQ), write SOPs, develop training materials, and maintain URS, risk assessments, and validation plans. Collaboration with cross-functional teams is essential to ensure audit readiness and
As a GMP Validation Writer: SOPs, Protocols & Compliance, you will play an important part at Sentry Bio Pharma Services, Inc. in Indianapolis, IN, United States.
We have an opening for a GMP Validation Writer: SOPs, Protocols & Compliance in Indianapolis, IN, United States within Bio & Pharmacology & Health, Engineering.
This role, GMP Validation Writer: SOPs, Protocols & Compliance at Sentry Bio Pharma Services, Inc., could be your next move.
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