S
Square Pharmaceutical, Inc
QC IP/FP Analyst
Skills
ComplianceRegulatory Compliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Cavite City, Cavite, Philippines
Work mode:
Onsite
Published on:
31 August 2026
What they need
Key responsibilities
- Inspect raw materials, in-process products, and finished goods for defects and deviations from specifications
- Document inspection results and provide detailed reports to help improve processes
- Ensure regulatory compliance with industry, safety, and regulatory standards
- Collaborate with production teams to identify potential quality issues early in the manufacturing process
- Maintain QC equipment and regularly calibrate tools used in quality inspections
- Implement corrective actions to improve product quality and prevent future defects
About you
- BS Chemistry, BS Pharmacy, BS Biochemistry, or BS Chemical Engineering graduate
- Preferably with experience in Laboratory or manufacturing
- Familiar with GLP and cGMP
- Knowledge in UV-vis Spectrophotometry operation and basic laboratory technique is a plus
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