Director Legal, Manufacturing Division

Role: Provide legal support on manufacturing compliance, including cGMP, to global biopharma operations, advising on quality, supply chain, and regulatory interactions. Responsibilities: review regulatory submissions, support regulatory inspections, draft and negotiate manufacturing-related agreements, and ensure compliance with cGMP standards. Requirements: JD from an accredited US law school, NJ Bar admission, 5+ years in regulatory law within law firms or corporate settings; experience with pharma or cGMP preferred. High-Value: pharmaceutical manufacturing, cGMP compliance, regulatory interactions (FDA, EMA), legal advising for quality and supply chain functions. WorkSetup: hybrid (3 days/week in Rahway, NJ or PA locations), with ~10% travel.