The Manufacturing Associate I/II is responsible for the execution of Upstream or Downstream production activities for early and late-phase Cell Culture programs within a GMP environment.
Requirements
- Manufacture cell culture products per manufacturing batch records in compliance with quality standards, company policies and current regulations.
- Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures.
- Document each task involving manufacturing procedures (i.e. SR’s, EPR’s and BR’s) following GDP at the time of execution.
- Ensure all items are issued and accounted for during the execution of a record (i.e. SR, EPR and BR)
- Demonstrate and apply understanding of current Good Manufacturing Practices (cGMP) and how they apply to specific tasks and responsibilities.
- Participate and be accountable for room 5S.
- Utilize and perform maintenance on equipment per applicable SOP.