- Preparation and review of the manufacturing and packaging Technical Direction.
- Preparation of SOPs pertaining to In-Process QA.
- Line Clearance during all critical process during Dispensing, Manufacturing, Filling & Stoppering and Packing operation.
- Verify the dispensing of RAW Material and Packing Material.
- In Process checking during dispensing , manufacturing, filling lyophillization, sealing, optical inspection, labeling and packing operation.
- Sampling of process Validation Batches.
- Sampling of In - Process and finished products and validation activities.
- Collection of swab and rinse sampling after cleaning of equipment's and area.
- Collection, Storage, Handling, Inspection and destruction of reserve samples.
- Review Executed Exhibit and commercial Batch Manufacturing Records and packaging Record for release of finished Product.
- To Monitor and verify any qualification of the process,



equipment and system.
- To Perform role of QA oversight and observe the compliance to SOP and aseptic behavior and indentify the deficiencies, if found any.
- To Excute the Aseptic Core Monitoring during batch processing activity.
- To participate in Media fill activities and ensure the review and compliance of the activity as per the Batch Records and protocols.
- Preparation of PQR data for the product manufactured in year on rolling basis.
- Collection and evaluation of Batch process parameters(CPP), Quality attributes from batch record and analytical record.
- To review the Non Viable trends of Production Area.
- To Perform any other works as and when assigned by HOD.

📌 Executive- QA (IPQA Injectable Plant) (Baddi)
🏢 Panacea Biotec
📍 Baddi