Director Legal, Manufacturing Division
Listed on 2026-10-09
-
Pharmaceutical
Regulatory Compliance Specialist -
Law/Legal
Regulatory Compliance Specialist
Provide legal support to manufacturing compliance (cGMP) and regulatory interactions within a biopharma context, focusing on quality, supply chain, and manufacturing agreements.
Responsibilities:advise on regulatory submissions, inspections, and compliance with cGMP; manage manufacturing-related legal risks and strategy; review regulatory documents and interactions with agencies like FDA/EMA.
Requirements:JD from an accredited US law school, admission to NJ or equivalent bar; 5+ years regulatory law experience, preferably in pharma or with cGMP expertise; strong communication, analytical, and multitasking skills.
High Value:experience with pharmaceutical manufacturing, regulatory agencies (FDA, EMA), and cGMP regulations; exposure to manufacturing compliance, regulatory inspections, and pharmaceutical law.
Work Setup:hybrid in NJ or PA (Rahway, North Wales, Upper Gwynedd); 10% travel.
Our team is growing, and we are hiring a Director Legal, Manufacturing Division in PA, United States.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).