Executive Quality Control - Formulation

Roles and Responsibilities

1. Analysis of In-process, Intermediates, Raw material, Packing material, Finished products, Stability study, Hold time study, Process validation, Cleaning samples, Vendor development and any analysis allocated by team leader and release with proper documentation..

2. Ensuring analysis is performed compliance to GLP.

3. Ensuring analysis raw data is documented on-line.

4. Initiation, Completion and filing of Daily analysis reports.

5. Ensuring any abnormal results, incidents, deviations, discrepancies are reported immediately to the reporting Section Head.

6. Ensuring all relevant log entries are made for every activity wherever applicable.

7. Supervise compliance to all cGMP, GxP or any other regulatory requirements including EHS requirements.

8. Report any quality concerns or suggestions for improvements to Department Head.

9. Execute and supervise all tasks and activities as per the applicable SOPs and company policy.

10. To maintain the safety norms while working in lab. (e.g. Wear goggles, PPE, Disposal of sample/media as per procedure etc).

11. Ensuring analysis is performed as per valid procedures and by using calibrated instruments / Standards.

12. Ensuring self-discipline with respect to wearing aprons, attendance and personnel hygiene and inter relations.

13. To perform Labware LIMS related activities.

14. Any other assignment given by the Section Head or Department Head.