About this role
(Sr.) Validation Engineer at GenScript/ProBio. Location: Pennington, New Jersey, United States. Role: executing CQV, developing protocols, maintaining documentation Requirements: BS/MS in life science, 9+ years GMP validation/engineering experience in drug/biologics, CQV experience, familiarity with CSV/GAMP 5 and 21 CFR Part 11, IQ/OQ/PQ protocol authoring, aseptic fill/finish experience preferred. Category: Engineering Seniority: Senior Level Tools: GAMP 5, 21 CFR Part 11, CSV Commitment: Full Time Workplace: Onsite Languages: English