QA Engineer - Medical Devices & Compliance

Variance Trading Corporation

Quezon City

On-site

PHP 300,000 - 420,000

Full time

7 days ago
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Job summary

Variance Trading Corporation in Metro Manila is seeking a Quality Assurance professional to help maintain compliance and document control in a regulated medical device environment.

You will assist with quality records, SOPs, CAPA, and internal audits, coordinating with departments to ensure quality standards are met. Candidates should have an engineering degree, familiarity with QMS, and strong MS Office skills.

Qualifications

  • Bachelor’s degree in engineering or related field within QA context.
  • Experience in Quality Assurance/Quality Control in regulated environments.
  • Familiarity with Quality Management Systems (QMS) and medical device standards is a plus.
  • Proficient in MS Office, especially MS Excel.

Responsibilities

  • Assist in preparing, organizing, and maintaining quality documents and records.
  • Support the preparation and updating of SOPs, forms, checklists, and other quality documents.
  • Assist in conducting quality checks and inspections as required.
  • Monitor compliance with established procedures and quality requirements.
  • Assist in documenting and investigating quality issues and non-conformities.
  • Support CAPA activities.
  • Assist with internal audits and follow-up of audit findings.
  • Coordinate with departments regarding quality concerns and documentation.
  • Prepare and maintain quality reports, monitoring sheets, and records.
  • Assist in monitoring product and process quality.
  • Help identify opportunities for process improvement and quality enhancement.
  • Perform other QA-related tasks as assigned.

Skills

Quality awareness
Attention to detail

Education

Engineering degree (Industrial/Chemical/Biomedical/Mechanical)

Tools

MS Excel
MS Office

Job description

Variance Trading Corporation in Metro Manila is seeking a Quality Assurance professional to help maintain compliance and document control in a regulated medical device environment.

You will assist with quality records, SOPs, CAPA, and internal audits, coordinating with departments to ensure quality standards are met. Candidates should have an engineering degree, familiarity with QMS, and strong MS Office skills.

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