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Forge Biologics is seeking a Director of Quality Control for Raw Materials to lead strategic and operational activities for the raw material testing program at their state-of-the-art 200,000-square-foot cGMP facility in Columbus, Ohio. This role manages the QC Raw Materials department and collaborates with internal Manufacturing, Supply Chain, Facilities, and Quality Senior Management, as well as external suppliers, to address quality-related issues.
Key responsibilities include providing strategic and operational leadership to the Quality Control department responsible for raw material sample receipt, incoming inspection and testing, and release of all starting materials (raw materials, consumables, etc.). The Director will develop and implement a material qualification program in a phase-appropriate fashion to support pre-clinical, clinical, and commercial manufacturing activities. Additional responsibilities include managing laboratory readiness, external testing oversight, and inspection-ready quality systems.
The role requires collaboration across departments to ensure quality standards are met and maintained. The Director will work with scientists, physicians, biotech and pharma innovators, and patient communities to support the development and delivery of life-changing gene therapies, particularly AAV manufacturing. This position is central to Forge's mission of enabling access to innovative gene therapies and bringing them from concept to reality.
Forge Biologics operates with a culture of H.O.P.E. (Hardworking, Open, Purpose-driven, Engaged) and is committed to employee growth through mentorship, hands-on learning, and advancement opportunities. The company focuses on improving lives through genetic disease treatments.
