Job Profile:

1. Responsible for prepare and execution of Annual Product Quality Review.

2. Responsible to initiate Change Control/Deviation/Non-conformance report/Corrective and preventive action/ Incident/Out of specification/Out of trend/Market complaint investigation.

3. Responsible to prepare process validation and bulk hold Time Study protocol and report.

4. Responsible for execution and compilation of process validation and bulk hold time study as per protocol.

5. Responsible for handling of visual inspector qualification activity.

6. To prepare and review standard operating procedures.

7. Responsible to maintain the document as per current positive manufacturing practices.

8. Responsible to provide the documents to regulatory department.

9. Responsible for co-ordination with internal as well as external department personnel.

10. Responsible for maintain and track the Process validation and Product bulk hold time study status

Desired Candidate Profile

- Candidate Should be from Pharma - injectable formulation background
- Should have knowledge of regulatory market
- Willing to work at location Pithampur , Near Indore (M.P)

Email Id : [email protected]

📌 Sr. Executive / Executive - QA (PV Profile ) - Indore Plant
🏢 Gufic Biosciences
📍 Indore