$125,740 – $152,368
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 commissioning and validation teams in a pharmaceutical manufacturing environment, managing projects, personnel, and regulatory compliance. It suits experienced professionals with deep expertise in GMP validation and strong management skills who want to advance in the regulated biotech sector.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
- Database Systems
- Microsoft Excel
- Microsoft Outlook
- Microsoft PowerPoint
- Microsoft Word
- SDLC Software Development Life Cycle
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What they ask for
Required
- Bachelor's degree in Engineering or Science
- 7+ years pharmaceutical application validation in GMP environment
- 7+ years managing personnel and projects
- Direct experience with regulatory audits
- Knowledge of cGMP in pharmaceutical industry
- Computer systems validation expertise
- Problem-solving and communication skills
Nice to have
- Experience with scheduling software
- Capital and expense budget forecasting experience
- Metrics creation and analysis experience