Providing all documents require for Regulatory Work.
To handle the queries raised against the submitted documents.
To ensure timely submission of documents to the authorities.
Issuance of Analytical worksheet, Protocol and formats.
Preparation and issuance of BMR and BPR.
Physical observation of retain samples as per schedule and documentation.
Archival of all master documents.
Destruction of retain samples after expiry.
To execute Destruction of records as per schedule.
To prepare Annual Product Review.
Candidates having experience in Pharmaceutical Formulation Industries.
Candidate criteria: