Description
The role is responsible for evaluating and validating manufacturing processes, cleaning procedures, aseptic filling, media fill, process qualification, continued process verification, cross-contamination risk assessments, deviations, validation reports, documentation archiving, and new-product transfer. It requires a bachelor’s degree in a scientific or pharmaceutical field, at least three years of direct experience in process validation, cleaning validation, or aseptic process simulation for sterile products, pharmaceutical production knowledge, risk management, project management, and advanced English communication skills.
