Graduate of BS Pharmacy, BS Biology, BS Chemical Engineering and any allied courses.- Have knowledge in ISO 9001:2015 Guidelines, Phil. FDA Manufacturing Guidelines, PIC/S Guide to GMP for Medicinal Products, WHO Guidelines in the Manufacture of Medicinal Products, Ethiopia Drug Administration Manufacturing Guidelines, Invima Drug Manufacturing Guidelines, Anvisa Drug Manufacturing Guidelines, other EU Regulatory Agency for the Evaluation of Medicinal Products.
Prepares the Quarterly Internal Quality Audit Schedule.
- Monitors, coordinates and follows up closure of all non-conformances observed during audits.
Must have strong communication skills.- Good in verbal and written documentation for audit reports.
Job Types: Full-time, Permanent
Benefits: Flexible schedule
Paid training- Transportation service provided
Schedule: 12 hour shift
Monday to Friday Shift system
Supplemental Pay:
* Overtime pay
