# Director, Regulatory CMC - Cell Therapy

Hiring organization: [Bristol Myers Squibb](https://career.thegoodapps.co/organizations/bristol-myers-squibb)

Canonical page: https://career.thegoodapps.co/jobs/de4bf983-e29f-4969-984b-9204407a25af

Listed on Bristol Myers Squibb's own careers site. Applications go to them directly.

- Employment type: full time
- Seniority: Director
- Salary: 199950 – 299287 USD per year

## Summary

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._

## 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

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Madison---Giralda---NJ---US/Director--Regulatory-CMC---Cell-Therapy_R1602987