• To perform In process checks, line clearance, sampling at appropriate stages (at semi-finished and finished product), during manufacturing and packing of products for cosmetic, and dental formulation.
• To follow GMP, GDP, Data integrity & safety principle in performing the defined Role & Work.
• To participate in validation activities (Process validation, Cleaning validation and Hold time sampling and qualification activities).
• To review of BMR/ BPR and release for next step of processing.
• To ensure that the Standard Operating Procedures are followed in day to day activity.
• To ensure that the environmental conditions are monitored in respective areas of the operation as per Standard Operating Procedure.
• Verification of raw material/packaging materials during dispensing.
• Maintaining IPQA records and ensures that records are updated as per procedure.
• To collect in process, intermediate and finished sample of the product being manufactured.
• Responsible for the Handling and management of Reserve samples and stability samples.
• Monitoring the area cleanliness and sanitation in manufacturing, packing, and warehouse.
• To ensure the proper status labelling to provide easy traceability and identification of material or product.
• Preparation and data collection of Annual Product Review.
• Issuance and Archival of documents from doc cell for compliance.
• Review of archived and issued documents from doc cell for compliance. (Issuance and Archival)
• Responsible for retrieval and archival of documents and updation of log books.
• Management of document  life cycle (Preparation, review, verification/ approval distribution, retrieval, withdrawal, obsolete) in DMS as per define procedures.
•  Any other work assigned by Team leader and Department Head.

B. Pharma.