Officer / Executive Aqa Job in Glenmark Pharmaceuticals Limited

Responsible for Review and approval ofValidation/Verification, Method validation, Analytical Tech Transfer protocoland reports. Ensure all results comply with specifications, compendia andregulatory requirements

Responsible for Logging, Review and Closing ofIncident/Deviation, CAPA, OOS, OOT & EP Investigation

Review, evaluation and Approval of investigationdocuments as a Designee of Head Investigation QA.

Verification ofAMV documents against STP (New / revision) during CC approval.

Responsible for Review and approval of the StabilityProtocol and Stability Summary Report.

Responsible for internal audit of Laboratory.

To Ensure the Compliance of SOP s of Quality controlDepartment. 10. To Provide Timely Support to Internal and External Customer asper the requirement.

To ensure the data integrity in each and everyreviewed document.