Associate Director, Aseptic & Sterile Process Engineering
Bristol Myers SquibbDevens, MA · full time · Director
$170,650 – $206,793
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 technical strategy for aseptic and sterile processing in an advanced automated cell therapy manufacturing environment, requiring deep expertise in contamination control, regulatory readiness, and process simulation. It suits experienced pharmaceutical or biotech engineers who can influence cross-functional teams and translate complex aseptic principles into automated manufacturing systems.
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 in Engineering, Biotechnology, Pharmaceutical Sciences, Microbiology, or related discipline
- Minimum 8 years in pharmaceutical, biologics, or cell and gene therapy manufacturing
- Hands-on experience with aseptic processing and sterile manufacturing operations
- Experience with contamination control strategies and environmental monitoring
- Direct experience leading or supporting Aseptic Process Simulations (media fills)
- Experience supporting regulatory inspections or commercial readiness activities
Nice to have
- Advanced degree (Master's or PhD) in relevant scientific or engineering discipline
- Experience with automated, robotic, or closed manufacturing systems
- Familiarity with mechanical sterile connectors or advanced aseptic interfaces
- Experience working with external equipment vendors or technology developers
- Strong written and verbal communication skills