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 Valuable 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

Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion.

📌 Assistant Manager, Quality Control (India)
🏢 Amneal Pharmaceuticals
📍 India