Location
caloocan, metro manila, Philippines
Posted
June 25, 2026
Job Description
Job Responsibilities
- Monitor regulatory updates, support compliance with GMP, ISO, FDA, and other applicable regulatory requirements.
- Checking and maintaining completeness and accuracy of quality records.
- Track CAPA implementation and report status to the QA/QC Manager.
Job Qualifications
- BS Chemistry, BS Biology, BS Pharmacy, BS Chemical Engineer or Allied Sciences.
- 1-2 years experience in QA/QC role in a manufacturing set-up.
- Knowledgeable in MS Office, with thorough knowledge and experience in handling documentation and compliances for ISO, FDA, and GMP requirements.
- Amenable to work on-site in Barangay Caybiga, North Caloocan
- CAN START ASAP