Associate Director Quality Systems

Role: Associate Director of Quality Systems at a new biotech manufacturing site, providing leadership for GMP compliance, quality systems, and regulatory adherence. Responsibilities: oversee critical quality issue escalation, review and approve quality documents (including deviations, change controls, vendor management, and document control), implement improvements in quality systems, supervise quality operations teams, and support site and corporate strategies. Requirements: BS in Pharmacy, Science, Engineering or related field; 8+ years in quality assurance within biopharmaceutical manufacturing; 4+ years of leadership experience. High-Value: experience with cGMP, FDA, EMA, Data Integrity, Quality Risk Management; quality systems expertise (e.g., TrackWise, automation tools); strong problem-solving and communication skills. Work setup: hybrid onsite in Richmond, VA, with 0-20% travel, including intra-site travel.