About this role
Senior Quality Process Validation Specialist at INCOG BioPharma Services. Location: Fishers, Indiana, United States. Role: overseeing validation, reviewing protocols, supporting audits Requirements: Bachelor's in science/engineering, 5+ years pharma/CDMO process validation experience, hands-on PPQ and CPV, CPP/CQA identification, statistical process monitoring, familiarity with FDA/EMA/ICH Q8-Q12 and technology transfer, audit support experience. Category: Quality Assurance Seniority: Senior Level Tools: Minitab, JMP Commitment: Full Time Workplace: Onsite Languages: English