Major Responsibilities
· Maintain records
- Ensure BMRs are complete and the necessary data are recorded in PC for PQR.
- Follow up of deviation controls and change controls, and completeness as per procedure.
- Follow up of proper documentation of training records.
· Revise documents
- Prepare PQR on products produced.
- Prepare/ review BMRs/BPRs for products and submit for approval.
- Revise formats and submit to immediate supervisor for check and approval.
· Participate in validation activities
- collect samples from validation batches at each sampling stages.
- Conduct the necessary test parameters on the samples.
- Ensure that samples of validation batches are submitted/ taken to QC lab.
- Participate in cleaning validation methods.
- Participate in validation of analytical methods.
· Perform IPQA activities
- perform IPQA activities and record results as needed as per the procedure, when assigned/required.
- To report non-conformances to immediate supervisor.
- Bachelor Degree in Pharmacy (B. Pharm) with Minimum 1- 3 years of related experience
- A very good English language skill of both writing and speaking is essential.