Director Legal, Manufacturing Division

Role: Provide legal support on manufacturing compliance, including cGMP, to biopharma manufacturing operations. Responsibilities: advise quality and supply chain teams, review regulatory submissions, support regulatory inspections, and advise on manufacturing agreements. Requirements: Juris Doctor from an accredited US law school, admission to NJ or other state Bar, 5+ years of regulatory law experience in law firm or corporate setting, strong communication and analytical skills. Preferred: cGMP and pharmaceutical industry experience, familiarity with FDA, EMA regulations, and regulatory interactions. HighValue: manufacturing compliance, cGMP, regulatory submissions, FDA/EMA engagement, hybrid work in NJ/PA, 10% travel.