About this role
Engineer Commissioning, Qualification & Validation (CQV) at Bristol Myers Squibb. Location: Leiden, South Holland, Netherlands. Role: writing protocols, executing qualifications, coordinating activities Requirements: BS in engineering/science preferred, 1+ years supporting pharmaceutical validation in a GMP environment; knowledge of cGMP/GxP/GAMP/SDLC/21CFR Part 11, strong communication and technical writing skills. Category: Engineering Seniority: Entry Level Commitment: Full Time Workplace: Onsite Languages: English