Documentation &
Document Control: Manage the complete lifecycle (preparation, issuance, retrieval, and destruction) of all QA documents, including SOPs, Logbooks, BMRs, and BPRs, while maintaining the documentation cell .
In-Process Quality Assurance (IPQA): Conduct line clearances, perform in-process checks, and execute Acceptable Quality Level (AQL) inspections across general manufacturing, packing, and aseptic areas .
Aseptic Area Oversight &
Media Fills: Provide strict QA oversight during aseptic processing, manage aseptic process simulations (media fills), and prepare related protocols, trend reviews, and personnel tracking matrices .
Sampling &
Dispensing Verification: Oversee sample collection for commercial, submission, and validation batches, and rigorously verify the dispensing of raw and packaging materials .
Shop-Floor Compliance &




Environmental Monitoring: Ensure strict cGMP compliance through frequent shop-floor rounds, monitor environmental controls/cleanliness, and verify routine equipment printouts (CIP/SIP, Autoclaves, incubators) .
Validation &
Qualification Execution: Actively participate in the preparation and execution of Process Performance Qualifications, Cleaning Validation protocols, Hold Time studies, and Master Formula Records (MFR) .
Product Reviews &
Audit Trails: Prepare Annual Product Quality Reviews (APQR), inspect finished product consignments, manage control samples, and review equipment audit trails for both aseptic and non-aseptic areas .

📌 Qa Sterile Assistant Manager Daman (India)
🏢 USV PRIVATE
📍 India