Quality Control Analyst - In-Process & Finished Product

Square Pharmaceutical, Inc

Carmona

On-site

PHP 279,000 - 391,000

Full time

3 days ago
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Job summary

Square Pharmaceutical, Inc. seeks a QC Inspector in Carmona, Cavite to inspect raw materials, in-process products and finished goods for defects and deviations, document results, and aid process improvements in a GMP manufacturing environment.

The role requires a BS in Chemistry, Pharmacy, Biochemistry or Chemical Engineering, familiarity with GLP and cGMP, calibration of QC equipment, and knowledge of UV-Vis spectrophotometry are a plus; candidates should be detail-oriented and able to

Qualifications

  • BS in Chemistry, Pharmacy, Biochemistry or 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.

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.

Skills

GLP
cGMP
Laboratory techniques

Education

BS Chemistry
BS Pharmacy
BS Biochemistry
BS Chemical Engineering

Tools

UV-Vis Spectrophotometer

Job description

Square Pharmaceutical, Inc. seeks a QC Inspector in Carmona, Cavite to inspect raw materials, in-process products and finished goods for defects and deviations, document results, and aid process improvements in a GMP manufacturing environment.

The role requires a BS in Chemistry, Pharmacy, Biochemistry or Chemical Engineering, familiarity with GLP and cGMP, calibration of QC equipment, and knowledge of UV-Vis spectrophotometry are a plus; candidates should be detail-oriented and able to

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