Job Description

Roles and Responsivities

Responsible to ensure planning and maintain high Quality standards in routine analysis.

1. To verify GLP requirement in laboratory.

2. Responsible for FDA related activities like new product licenses, notices and audits related response are timely completed.

3. Planning of calibration & AMC related activity as per planner and ensuring compliance.

4. Planning of raw materials, FP and stability testing as per priority.

5. Ensuring reagents, laboratory chemicals are properly labeled.

6. Review of related methods & requirements of products and client response.

7. Preparations and updating of departmental SOPs as per requirements.

8. Ensure working standard management and qualifications.

9. Generation of PRF related to Quality control requirements and verify timely submission of bills.

10.Checking and review of inventory related to laboratory regents and glassware.

11.Control samples arrangement in control sample room.

12.Inspection plan attachments in SAP for new products or after any updation.

13.To participate in 1s and 2s activities in plant

Desired Candidate Profile

M.Sc. (Chemistry) M pharma from Pharma Industry