Summary from listing
The Validation Manager leads and supports validation projects for equipment, facilities, utilities, processes, and computer systems used in pharmaceutical manufacturing. The role owns data integrity and computerized system validation activities, including CSV/GAMP, 21 CFR Part 11, Annex 11, risk assessments, data stream mapping, remediation, audits, investigations, validation plans, protocols, and project execution. It also provides technical guidance to improve validation team performance and quality processes, requires a BS in engineering, chemistry, microbiology, or a related field, and requires 5–7 years of related industrial validation experience.
