Assistant Manager, Quality Control

Responsible for Review of Quality Control documents and Electronic data.

•Responsible for initiation, review and investigation related to Deviations, OOS, OOAL, CAPA & LIR.

•Responsible for Review of documents related to GLP, Raw material, Packaging material, Inprocess, Finished, Stability and Miscellaneous.

•Responsible for preparation and review of Quality control SOP, GTP, STP and Specifications.

•Responsible for maintaining of Good laboratory practices in the lab.

•Responsible for maintain of regular cleanliness of laboratory.

•Responsible for overall management of Laboratory compliance.

•Responsible for Review of Volumetric solutions, Limit Test solutions, Test solutions, LNBs, CoA's and all other test reports.

•Responsible for Review of calibration reports of Instruments and Equipments as and when required.

•Responsible for initiating and review of Change controls and Deviations.

•Responsible for review and preparation of Method verification Reports/Protocols.

•Responsible for review of Method verification activities.

•Responsible for checking the maintenance of Columns, reference standards and Working standards.

Qualification - B.Pharmacy, M.Pharmacy