The Role is responsible for reviewing the Batch Production Record, Issuance and Reviewing the Product Labels
Release of finished products, Verification activities of finished goods at the sites.
Key Individual Accountabilities
Handing & tracking of QMS related activities CAPA, Deviations, Customer Complaints. OOS/OOT, Investigations
Ensure timely review of Batch Production record, Review & approval of investigation, verification of CAPAs, review of QC test results, batch disposition quarantine, rejections approval
Release/Rejection of finished products as per approved specifications
Calibration &
Maintenance QA oversight
To perform cleaning verification during product change over and dispatch verification of finished as per established procedures
Verification of reprocessing activities in the site
Handling of Sale Returns
Complying to the laid down norms of Safety Health &
Enviroment
Any job assigned time to time by superior based upon training on the procedure
Requirements
Required Competencies
Working with People
Relating &
Recent working
Adhering to principles &
Values
Adapting & responding to changes
Coping with Pressure &
Setbacks
Achieving Personal work Goals &
Objectives
Have the Exposure of Audits.
Education M.Sc. in Chemistry/ M.Pharma
Experience: 10 to 15 years. (Candidate should have API Experience)