Associate Director CMC Regulatory Affairs
Regeneron Pharmaceuticals(12 days ago)
About this role
The Associate Director, CMC Regulatory Affairs leads global regulatory strategies for combination products and medical devices, specifically focusing on ex-US markets. The role involves providing regulatory expertise, supporting development and approval processes, and collaborating across cross-functional teams in an international environment.
Required Skills
- Regulatory Affairs
- Global Regulations
- Medical Devices
- Combination Products
- EMA
- Notified Bodies
- Technical Writing
- Risk Management
- Strategic Planning
- Cross-functional Collaboration
About Regeneron Pharmaceuticals
regeneron.comDiscover how Regeneron (NASDAQ: REGN) harmonizes biology and technology to create life-changing medicines. Join our team and explore clinical trials.
View more jobs at Regeneron Pharmaceuticals →Apply instantly with AI
Let ApplyBlast auto-apply to jobs like this for you. Save hours on applications and land your dream job faster.
More jobs at Regeneron Pharmaceuticals
QA Validation Specialist
Regeneron Pharmaceuticals(6 days ago)
Temp QC Analyst (HPLC/Micro/Tech Resource)
Regeneron Pharmaceuticals(6 days ago)
Process Development Engineer III Analytics Automation
Regeneron Pharmaceuticals(6 days ago)
Director, Culture & Inclusive Science
Regeneron Pharmaceuticals(6 days ago)
Similar Jobs
Senior Director, Regulatory Affairs CMC
Mirum Pharmaceuticals(7 days ago)
Director Regulatory Affairs, CMC
Bavarian Nordic(2 months ago)
Regulatory Affairs Manager - Vascular (on-site)
Abbott Laboratories(19 days ago)
Manager, CMC Regulatory Affairs
Capricor Therapeutics(19 days ago)
Regulatory Affairs Project Manager / Regulatory Affairs Manager
Roche(5 days ago)
Senior Regulatory Affairs Director
Medtronic(17 days ago)