Quality Manager – Sterile Manufacturing

Support batch review and release activities by reviewing GMP documentation and manufacturing records. Manage deviations, CAPAs, and change controls while providing quality support to production, laboratories, and warehouse operations. Maintain strong shopfloor presence to drive continuous improvement and act as the compliance contact for customers and external partners. Support inspections and client audits in this specialized sterile pharmaceutical manufacturing site. This role offers high visibility within a highly regulated environment with broad responsibilities directly impacting operations.