# Associate Director, Global Regulatory Sciences - CMC

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

Canonical page: https://career.thegoodapps.co/jobs/d6561c3a-a1ee-4b8e-b62d-aa33152b0316

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

- Employment type: full time
- Seniority: Senior
- Salary: 164020 – 198759 USD per year

## Summary

This role involves developing and managing regulatory compliance documentation for pharmaceutical and cell therapy products across their lifecycle, from clinical trials through post-approval. It suits experienced regulatory professionals who can independently guide technical teams on complex CMC requirements and interface with health authorities on submissions.

_Our summary, not Bristol Myers Squibb's wording._

## Skills named

Project Management

## Required

- Bachelor's degree
- 8+ years pharmaceutical industry experience
- 5+ years CMC regulatory strategy experience
- Knowledge of CMC regulatory requirements for advanced therapies, small molecules, biologics, and cell therapy
- Ability to independently manage complex projects with minimal supervision
- Experience leading teams and representing regulatory functions across project teams
- Strong written and oral communication skills
- Experience with regulatory submissions and dossier systems

## Nice to have

- Knowledge of small molecules, biotechnology, or cell therapy products
- Expertise in biological or cell therapy modalities and drug development processes
- Experience developing and documenting regulatory strategies in coordination with clinical plans
- Experience facilitating issue resolution and conflict management

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Princeton---NJ---US/Associate-Director--Global-Regulatory-Sciences---CMC_R1604324-1