Manager, GLP Compliance

Role: Manager, GLP Compliance supporting laboratory operations in a biopharma setting focused on autoimmune disease therapies, including cell and gene therapy. Responsibilities: ensure GLP compliance across laboratory activities, develop and improve quality control processes, support audits and inspections, manage documentation, provide GLP training, and promote continuous quality improvement. Collaborate with cross-functional teams such as Clinical Operations, Regulatory Affairs, and vendors to maintain inspection readiness and foster a culture of quality. Requirements: Bachelor's in Life Sciences or related field, at least 2 years of experience in biopharma/lab operations within GxP environments, supporting document control, and familiarity with GLP, GCP, ICH guidelines, and FDA regulations. Preferred: experience with cell and gene therapy. High-value: supporting GLP compliance in a clinical-stage biotech advancing autoimmune therapies, including CAR T-cell products, with a focus on regulatory adherence, documentation, audit readiness, and cross-disciplinary collaboration. Work Setup: remote based in Philadelphia, PA.