Sentry BioPharma Services in Indianapolis seeks a detail-oriented Validation Technical Writer to join our Validation team. You will ensure accuracy, clarity, and regulatory compliance across GMP documentation, supporting IQ/OQ/PQ, SOPs, URS, risk assessments, and lifecycle plans.
The role requires a scientific/technical background, 3 years in technical writing in life sciences, GMP exposure, and ability to collaborate with cross-functional teams to deliver compliant documentation and auditable
#J-18808-LjbffrGMP Validation Technical Writer — Protocols & SOPs Expert in indianapolis at Unknown Company
This position is listed as full time and onsite.