Supervisor, Production Operations

The Production Supervisor supports the timely manufacturing of parenteral products in an aseptic environment according to Current Good Manufacturing Practice (cGMP). The role involves supervising sterile filling equipment setup, operating dehydrogenation equipment, managing filling and capping processes, and overseeing formulation tasks. The supervisor ensures compliance with regulations, maintains good documentation practices, and participates in training and continuous improvement initiatives. Additionally, the role requires supervising sanitation of aseptic areas and adhering to sanitization protocols for sterile equipment processing.