
Director, Drug–Device CMC Reg Affairs (Autoinjector)
Merck, Springfield, IL, United States
A global biopharmaceutical leader is seeking a Director/Principal Scientist for Devices and Drug-Device Combinations Regulatory CMC. The role involves leading strategies for regulatory affairs, managing compliance for autoinjector and inhalation products, and ensuring technical quality of submissions. Candidates should have over 10 years of experience in biological or pharmaceutical research, alongside strong communication and leadership skills. This position offers a hybrid work model and comprehensive benefits package with a competitive salary range.
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