$106,630 – $129,214
Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role leads equipment validation and computerized system management for a cell therapy manufacturing site, overseeing both technical execution and team development. It suits experienced pharmaceutical professionals who combine hands-on qualification expertise with supervisory capability and a grasp of FDA compliance requirements.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree or equivalent experience
- Minimum 5 years in FDA-regulated industry
- Strong understanding of cGXP and good documentation practices
- Working knowledge of ISPE guidance and 21 CFR Part 11
- Working knowledge of SDLC principles
- Ability to document User and Functional Requirements
- Knowledge of pharmaceutical laboratory and manufacturing systems
- Experience executing equipment qualification documents
- Ability to interact with manufacturing, QA, and Facilities teams
- Strong MS Windows knowledge
- Ability to manage multiple concurrent tasks
- Strong written and verbal communication skills
- Proficiency in Microsoft Office Suite
- Hands-on leadership of direct reports
Nice to have
- Experience with pharmaceutical laboratory and manufacturing systems implementation
- Research and development of validation tools and solutions
- Standardization and review of validation deliverables