Regulatory CMC & Digital Transformation Lead

A global healthcare company in New Jersey is looking for an Associate Director, RACMC to oversee regulatory Chemistry, Manufacturing, and Controls for drug projects. The role includes organizing submissions, managing digital transformation initiatives, and leading cross-functional teams. Candidates should have at least 7 years in the pharmaceutical industry with expertise in regulatory affairs. A Bachelor's in Life Science is required, while a Master's or PharmD is preferred. Travelling up to 10% may be expected.
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