The Downstream Processing Supervisor oversees biopharmaceutical manufacturing processes, including chromatography, viral inactivation, filtration, ultrafiltration, and aseptic filling.
Responsibilities include executing batch records and SOPs, maintaining equipment and documentation, managing supply chain issues, investigating deviations, and ensuring compliance with cGMP standards.
They lead shift operations, coordinate training, build team relationships, and provide feedback for continuous improvement.
Required skills include 5-9 years in cGMP manufacturing, 2+ years in a supervisory role, knowledge of aseptic techniques, and proficiency in MS Office.
The role involves working in cleanroom environments on rotating night shifts, requiring gowning, lifting, and standing for extended periods.
Compensation ranges from $43.00 to $48.00/hr, with benefits such as health coverage, retirement plans, and PTO.
This is a full onsite position in Saint Louis, MO, with an application deadline of May 5, 2025.