QA Operations Engineer for GMP biopharmaceutical manufacturing floor oversight and batch quality.
Embedded QA role supporting on-site batch record review, deviation/CAPA management, and automation exception handling in a regulated biologics manufacturing environment. Requires 8+ years of GMP biopharmaceutical operations experience, regulatory knowledge (21 CFR 210/211, EU GMP), and ability to work full-time on-site in Switzerland. Strong technical foundation in batch record systems and deviation investigation essential.
Membership is €29/month, cancel anytime: every rate, every original listing link, and a daily alert for roles matching your filters.
Found at a specialist agency · listed 21 October 2026 · InsideJobs links you to the original posting.