The position requires a graduate of Industrial Engineering, a Bachelor in Pharmacy/Chemistry, or any related courses. Experience in quality assurance of drug products and knowledge in GMP is an advantage.
Duties and Responsibilities:
- Checks and monitor process area prior to start of manufacturing as to fitness for product processing
- Direst QA Assistant Inspectors in conducting checks in the processing and storage areas
- Ensure quality of manufactured goods by monitoring the manner routine in-process checks, e.g. quick visual inspections, leakers test, compressed tablet parameters check, etc. are done
- Observe dials, gauges, indicators, etc. to make sure that a machine is working properly
- Routinely checks storage areas to ensure correct storage conditions are met
- Monitors products processes and personnel on the adherence to good manufacturing practice (GMP)
- Monitors the performance of quality systems and procedures
- Monitors Manufacturing/Packaging Batch Record (MBR/PBR) trail to ensure that process are well documented and traceability is maintained.
Job Type: Full-time
Pay: Php17,000.00 - Php18,000.00 per month
Benefits: - Company events
Employee discount Life insurance
- Opportunities for promotion
Promotion to permanent employee
Schedule:Supplemental Pay: Overtime pay
Ability to commute/relocate:
* San Mateo, Rizal: Reliably commute or planning to relocate before starting work (Required)
