QC/QA Analyst: Precision Quality & Compliance

Columbia International Food Products

Navotas

On-site

PHP 260,000 - 360,000

Full time

14 days+
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Job summary

Columbia International Food Products is seeking a QC/QA Analyst for on-site work in Navotas. The role requires a Bachelor’s degree in Chemistry or related field and 1–2 years of QC/QA experience in manufacturing. Licensing as Chemist or Technician is preferred.

You will conduct tests, review results, calibrate instruments, and help ensure GMP and regulatory compliance. Responsibilities include QA system implementation, batch record review, CAPA, internal audits, and maintaining thorough

Qualifications

  • Bachelor’s degree in Chemistry, Chemical Engineering, or related field.
  • Licensed Chemist or Chemical Technician preferred or required depending on industry.
  • At least 1–2 years experience in QC/QA within a manufacturing environment.

Responsibilities

  • Conduct chemical, physical, and microbiological tests on raw materials, in-process batches, and finished goods.
  • Review test results and verify conformance to established specifications.
  • Document analytical data, deviations, and abnormalities with accuracy and traceability.
  • Calibrate laboratory instruments in accordance with SOPs and regulatory requirements.
  • Implement QA systems, including GMP compliance, process validation, and documentation control.
  • Review batch production records, test results, and supporting documents before release.
  • Participate in root-cause analysis and implement CAPA.
  • Conduct internal quality audits and assist with external regulatory inspections.
  • Maintain complete and compliant laboratory and QA documentation.
  • Generate QC/QA reports, trend analyses, and stability data summaries.

Job description

Columbia International Food Products is seeking a QC/QA Analyst for on-site work in Navotas. The role requires a Bachelor’s degree in Chemistry or related field and 1–2 years of QC/QA experience in manufacturing. Licensing as Chemist or Technician is preferred.

You will conduct tests, review results, calibrate instruments, and help ensure GMP and regulatory compliance. Responsibilities include QA system implementation, batch record review, CAPA, internal audits, and maintaining thorough

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