QA INSPECTOR (LINE)

Greenstone Pharmaceutical H.K., Inc.; Imus; On-site; PHP 250,000 - 350,000; Full time

Job summary

Greenstone Pharmaceutical H.K., Inc. in Cavite, Philippines invites applicants for a production quality-assurance role focused on in-process inspections across manufacturing, compounding, filling, coding, labeling and packaging operations.

You will verify compliance with Batch Manufacturing Records (BMRs), SOPs, logbooks and control parameters; coordinate with Quality Control for testing and result review; document deviations, incidents and quality observations; assist CAPA actions and support

Responsibilities

• 1. Perform in-process inspections during manufacturing, compounding, filling, coding, labeling, and packaging operations.
• 2. Perform line clearance checks and material verification before and during operations.
• 3. Verify adherence to approved Batch Manufacturing Records (BMRs), SOPs, logbooks, and control parameters.
• 4. Ensure compliance with GMP requirements and regulatory guidelines.
• 5. Coordinate with Quality Control for testing and result review.
• 6. Initiate and document deviations, incidents, and quality observations as required.
• 7. Assist in implementing and verifying corrective and preventive actions (CAPA).
• 8. Support audits, inspections, and continuous improvement initiatives.
• 9. Monitor critical process steps and immediately report deviations or non-conformances.

Job description

• 1. Perform in-process inspections during manufacturing, compounding, filling, coding, labeling, and packaging operations.
• 2. Perform line clearance checks and material verification before and during operations.
• 3. Verify adherence to approved Batch Manufacturing Records (BMRs), SOPs, logbooks, and control parameters.
• 4. Ensure compliance with GMP requirements and regulatory guidelines.
• 5. Coordinate with Quality Control for testing and result review.
• 6. Initiate and document deviations, incidents, and quality observations as required.
• 7. Assist in implementing and verifying corrective and preventive actions (CAPA).
• 8. Support audits, inspections, and continuous improvement initiatives.
• 9. Monitor critical process steps and immediately report deviations or non-conformances.