Executive

2 weeks ago


Ankleshwar, India Sun Pharmaceutical Industries Ltd Full time

1

Handling of Change Control/Planned Deviation.

2

Reviewing of new/ revised BMR/SDR/ECR.

3

Preparation and reviewing of QMS documents based on requirement.

4

Handling of Technology transfer

5

Monitoring of Engineering compliance. Monitoring, Reviewing and Approving scheduled activity and participation in associated activity for Qualification, Calibration and Validation.

6

Preparation, Execution, Monitoring, tracking and Review of Process and Cleaning Validation related activities.

7

Responsible for ensuring GxP compliance at site. To verify the current practices against the Standard procedures specified in SOP.

8

Monitoring and tracking of various compliance actions arising due to external/internal audits including activity involved in inspections.

9

Supportive role during inspections at site.

10

Other activity instructed from time to time.


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