Global Regulatory Affairs CMC Lead – Hybrid

A leading biopharmaceutical company in Boston seeks an experienced Regulatory Affairs professional to manage global regulatory CMC strategies. The role involves developing submissions, ensuring compliance with regulatory standards, and communicating with Health Authorities. Candidates should possess a strong background in scientific regulatory requirements, with at least 10 years of industry experience and an advanced degree preferred. This position offers a hybrid work model, competitive salary, and comprehensive benefits.
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