$123,580 – $149,752
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
Lead technical strategy and lifecycle management for sterile biologic drug products across manufacturing sites, ensuring process robustness and regulatory compliance. This role suits scientists with deep expertise in aseptic processing and biologics manufacturing who can drive cross-functional projects and influence decisions in matrix organizations.
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 and 9+ years relevant experience in drug product manufacturing
- In-depth knowledge of biologics and sterile liquid drug products
- Experience in aseptic drug product manufacturing and/or technology transfer
- Ability to serve as technical expert for manufacturing sites
- Critical thinking and technical writing skills
- Ability to work independently with limited supervision
- Experience working effectively in matrix environments
- Demonstrated ability to build alignment across analytical, regulatory, and manufacturing partners
- Demonstrated ability to influence areas outside direct control
Nice to have
- Master's or Ph.D. degree
- Experience in lyophilization technology
- Thorough knowledge of quality systems and validation principles
- Working competency in Statistical Process Control
- Experience with regulatory filings and Health Authority interactions