Assistant Manager, Quality Control

About the role

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.

What you'll do

• 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

What you need

• Quality control
• GLP
• SOP writing
• Calibration
• Maintenance
• Learning and development
• B.Pharm or M.Pharm

Good to have

• Performance management