GMP Manufacturing Associate

Role: GMP Gene Manufacturing Associate I/II responsible for producing clinical and commercial adenovector products in a cGMP setting. Core responsibilities include assembling raw materials, executing Master Batch Records, supporting SOP development, managing deviations, and ensuring equipment cleanliness and changeovers. The role entails participation in technology transfer and working within a cross-functional team while adhering to safety and regulatory standards. Requirements: Bachelor's or Master's in biology, biomedical science, or life sciences; 1-3 years GMP manufacturing experience; aseptic technique expertise. Preferred: prior cell culture/purification experience, TFF familiarity. HighValue: GMP manufacturing, adenovector gene therapy products, clinical and commercial phases, cGMP compliance, SOP development, deviation management. Work setup: on-site with occasional weekend and shift work.