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Global Regulatory Affairs Director — Submission PM Lead

Kailera Therapeutics, Inc., Waltham

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A progressive biotechnology company is seeking a Director of Global Regulatory Affairs in Waltham, MA. This role involves leading cross-functional teams to execute compliant marketing authorization submissions for product approvals. The ideal candidate will have over 10 years of regulatory affairs experience and a proven track record in managing global submissions. Responsibilities include strategizing submission plans, ensuring compliance with global regulations, and managing project timelines. Comprehensive health coverage, flexible time off, and a substantial salary range are offered.
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