$199,950 – $299,287
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 director-level role oversees chemistry, manufacturing, and controls strategies for cell therapy products at a major pharmaceutical company, involving regulatory submissions, cross-functional leadership, and health authority engagement. The position suits experienced pharmaceutical regulatory professionals with deep CMC expertise in advanced therapies who can guide teams through complex global approval processes.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
What they ask for
Required
- Bachelor's degree in a relevant field
- Minimum 10 years pharmaceutical or related industry experience
- Minimum 8 years of regulatory CMC experience
- Knowledge of CMC regulatory requirements for advanced therapies and cell therapy
- Experience leading cross-functional teams
- Direct experience developing strategy and leading teams through health authority interactions
- Strong knowledge of global regulatory agencies, policies, and guidelines for drug development
- Experience as member of CMC teams or comparable regulatory project experience
Nice to have
- Multidisciplinary pharmaceutical background
- Prior management experience
- Experience with product partnerships including out-licensing, divestiture, co-development, in-licensing, and acquisitions