GMP Validation Writer: SOPs, Protocols & Compliance

Sentry BioPharma 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