Join a team that provides critical QA oversight in cell therapy manufacturing, ensuring compliance and quality at every step. Lead QA operations, support manufacturing processes, and drive continuous improvement in a dynamic, GMP-regulated environment.

Lead and develop a team of scientists ensuring high-quality analytical support for pre-commercial and commercial projects in a dynamic laboratory environment, while maintaining compliance with industry regulations and operational excellence.

Lead teams to ensure efficient upstream manufacturing processes while fostering a culture of quality, safety, and compliance. Provide coaching and support to enhance team performance and drive continuous improvements across operations.

Manage and lead daily Pharmaceutical Development and Clinical Manufacturing operations, ensuring compliance and efficient execution of oral solid dose projects through strong team oversight and cross-functional coordination.

Advance facility operations by ensuring reliability of utilities and equipment, managing maintenance budgets, and leading compliance with regulations to support efficient pharmaceutical manufacturing processes.