Associate Principal Scientist (Assoc. Director), Regulatory Affairs - CMC
MSDNew Jersey, United States • Rockville, Maryland, United States • Upper Gwynedd Township, Pennsylvania, United States
Posted March 17, 2026
142400 - 224100 USD
Full Time
About the Company
Merck & Co., Inc. is a global healthcare company that embraces diversity and inclusion.
Job Description
We are seeking an Associate Principal Scientist (Assoc. Director) for our Global Regulatory Affairs & Clinical Safety (GRACS) team. The successful candidate will be responsible for developing and implementing CMC regulatory strategies for our pharmaceutical pipeline products, with a focus on small molecule respiratory/inhalation product development.
Requirements
- B.S. in a biological science, engineering, or a related field
- At least five (5) years of relevant experience in biological/pharmaceutical research, manufacturing, testing, or regulatory CMC
- Regulatory CMC experience with complex drug-device combination products/inhalation products
- Ability to develop innovative and imaginative approaches to problem solving and flexibly respond to changing priorities or unexpected events
Benefits
- Medical, dental, vision healthcare and other insurance benefits
- Retirement benefits, including 401(k)
- Paid holidays, vacation, and compassionate and sick days
- Annual bonus and long-term incentive
- Comprehensive package of benefits