Senior Director, Global CMC Regulatory Affairs

A clinical stage biopharmaceutical company is seeking a Regulatory CMC professional to provide global support throughout product lifecycle. Key responsibilities include managing high-quality regulatory submissions and overseeing regulatory activities. The ideal candidate will hold a Ph.D. in a relevant field with 5-10 years of regulatory CMC experience in the biotech or pharma industry. Strong project management and communication skills are essential for success in this role located in Gaithersburg, Maryland.
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