About the role

Anagram Therapeutics, Inc. in Natick, MA is seeking an experienced Associate Director to lead Regulatory Affairs CMC across development and lifecycle stages. You will plan submission strategies, prepare CMC documents for INDs/NDAs/BLAs, and collaborate with cross-functional teams to ensure compliant, timely filings while navigating evolving regulatory requirements. Lead regulatory strategy, guide teams through Module 3, and drive inspections readiness in a fast-paced biotech setting.

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JOB OVERVIEW

Experience level

Manager

Location

Natick, MA

Occupation

Regulatory Affairs Managers

Industry

Research and Development in Biotechnology (except Nanobiotechnology)

Posted

yesterday

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