Los Angeles, California
•
Today
Key Responsibilities Develop and execute IQ/OQ/PQ protocols for critical manufacturing processes.Conduct process characterization using DOE, SPC, and statistical modeling.Perform process capability studies (Cp/Cpk) and implement corrective actions for lowcapability processes.Define and maintain the Process Validation Master Plan (PVMP).Prepare validation protocols, reports, risk assessments, PFMEAs, and process maps.Support pilottoproduction scaleup for new blood glucose sensor manufacturing lin
Easy Apply
Contract
Depends on Experience











