Principal Scientist (Director), Regulatory Affairs-CMC
MSDNew Jersey, United States • Rockville, Maryland, United States • Upper Gwynedd Township, Pennsylvania, United States
Posted March 17, 2026
190800 - 300300 USD
Full Time
About the Company
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
Job Description
Principal Scientist (Director) for Regulatory Affairs-CMC, leading oversight of multiple programs in Respiratory franchise and some conventional small molecule programs, responsible for developing and implementing CMC regulatory strategies for pharmaceutical pipeline products.
Requirements
- Regulatory leadership and oversight
- CMC regulatory strategy development
- Global Regulatory CMC strategy execution
- Regulatory submissions preparation
- Leadership and management of team members
- Problem-solving and decision-making
Benefits
- Comprehensive benefits package
- Medical, dental, vision healthcare, and other insurance benefits
- Retirement benefits, including 401(k)
- Paid holidays, vacation, and compassionate and sick days