Job descriptionResponsible for driving excellence in sterility assurance practices, meeting the global regulatory requirements, drive sterility Assurance Program at siteConduct sterile quality management review periodicallyPeriodic review and routine check of classified areas like manufacturing, Microbiology and utility areasPreparation & adherence to Sterility Assurance Calendar consisting of Review timelines, training calendar and requalificationEnsuring SOP adherence to clean room facility / utilities / equipment / Personnel qualifications whichever has a potential to impact the Sterility of the product.Review validation / protocol studies which has potential to directly or indirectly impact the sterility of the productOversee the media fill programOversee the microbial OOS and OOT investigations, ensure microbial excursions are adequately handled and investigatedEnsure microbial trend data is analyzed and actions are taken proactively.Environmental Monitoring (EM)Personnel MonitoringMedia Fill Simulations (Process Simulations)Change controls related to Facility / Process / Utilities which may impact the current validated state with a focus on SterilityEnsuring periodic training of personnel involved in Sterility process and ensure practices to be followed while ensuring desired behavior on shop floorEnsure the microbial testing at the laboratory meets the appropriate guidance and pharmacopeiaEnsure the microbial data generated in laboratory is used meaningfully for plant operationsOversight of aseptic interventions, gowning qualifications, and contamination control strategiesEnsure appropriate Data Integrity controls are applied and followed