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.
Required Competencies:
Working with People
Relating & Current 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)