Moderna Therapeutics is seeking an Associate Director of Global Regulatory Affairs, CMC, to oversee CMC and Quality agency correspondence and regulatory applications for global products.
You will lead regulatory activities, ensure high-quality CMC sections, and manage multiple projects in a fast-paced environment to advance transformative medicines. This role supports a 70/30 in‑office work model and a collaborative, in-person culture.
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This position is listed as full time and onsite.