Title: Manager - 2 Engineering QMS
Date:
Jun 6, 2025
Location:
Halol - Engineering
Company:
Sun Pharmaceutical Industries Ltd
|
Engineering GMP Documents. |
Qualification Documents. |
Break down/Preventive maintenance report. |
QMS documents review and closing. |
Any other documents related to QMS. |
- Ensure that Engineering QMS Documents (Deviation, CAPA & CC) are closed within timeline.
- Implementation of CAPA within time limit.
- Tracking of department QMS documents ((Deviation, CAPA & CC)
- Preparation of GMP and QMS record.
- Preparation of Internal and external audit Compliance report.
- Participate in engineering investigation.
- To impart required training to concern persons.
- Participate in monthly Quality Review board meetings and update status of Eng. CAPA, Deviation and Change control.
- Coordination with cross functional department for closing of QMS documents.
- To ensure that department biannual due SOPs are revised before due date.
- To update the status of issued Qualification protocol on monthly basis.
- To ensure timely closing of FMS and EDMS issued forms.
- Ensure timely completion of SOPs training.
- Tracking and Handling of training related activity.
- Ensure timely retrieval of SOP from QA and maintain the SOP Index.
- Documents are maintain as per SOP.