Lansdale, Pennsylvania
•
Today
Develop, execute, and maintain Cleaning Validation protocols, reports, and lifecycle documentation for pharmaceutical manufacturing equipment and process systems. * Perform cleaning validation studies, including swab, rinse, visual inspection, and recovery sampling, to demonstrate equipment cleanliness and compliance. * Establish scientifically justified cleaning acceptance limits using HBEL, PDE, ADE, and MACO calculations. * Conduct risk assessments to identify worst-case products, equipment,
Easy Apply
Contract
Depends on Experience