About this role
6445 - Lead CQV SME / Lead Validation Engineer at Verista, Inc.. Location: Devens, Massachusetts, United States. Role: providing governance, mentoring engineers, reviewing deliverables Requirements: Bachelor's degree and 15+ years GMP CQV experience across complex biologics/sterile facilities; deep knowledge of ASTM E2500, ISPE, GAMP5, FDA/EU Annex15; strong technical writing and mentorship skills. Category: Quality Assurance Seniority: Senior Level Tools: ValGenesis Commitment: Full Time Workplace: Onsite Languages: English