About this role
Validation Associate Engineer at Bristol Myers Squibb. Location: Bothell, Washington, United States. Role: supporting review, generating protocols, performing assessments Requirements: Bachelor's in life sciences/engineering/STEM, 2 years GMP experience, experience or exposure to CQV, knowledge of cGMP/GDP/GxP/GAMP5/21CFR Part 11, strong technical writing, project management, and experience with validation lifecycle and electronic document management. Category: Engineering Seniority: Entry Level Commitment: Full Time Workplace: Onsite Languages: English