Compliance Officer – Medical Devices (EMS)

Grupo TECMA · tijuana, tijuana, Mexico

Location
tijuana
Job Type
Full-time
Posted
June 19, 2026

Job Description

Quality & Regulatory Compliance
  • Own and maintain the site Quality Management System (QMS) in alignment with:
  • FDA QMSR (21 CFR 820 – ISO 13485:2016 aligned)
  • ISO 13485 and applicable global regulations
  • Monitor and implement regulatory updates (FDA, ISO, international) and translate them into actionable site requirements.
  • Ensure QMS documentation is current, effective, and audit-ready.
Audits & Inspections
  • Lead and host:
  • FDA inspections
  • ISO / registrar audits
  • Customer audits (medical device OEMs)
  • Own audit preparation, execution, response, and closure.
  • Develop and track CAPAs to ensure root cause effectiveness and prevention of recurrence.
Risk Management & CAPA
  • Ensure robust risk management practices across:
  • Manufacturing processes
  • Material changes
  • Supplier changes
  • Lead invest...

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