Quality Engineer - Medical Devices | Process & Compliance

Grupo TECMA

Ciudad Juárez

Presencial

MXN 334.800 - 558.000

Jornada completa

14 días+

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Descripción de la vacante

A leading company in the medical device sector in Ciudad Juárez is seeking a Process Quality Engineer to ensure regulatory compliance and process stability in controlled manufacturing environments. The ideal candidate will hold a Bachelor's degree in Engineering and possess at least 3 years of experience in the medical device industry, with strong knowledge of ISO 13485 and quality tools. This role requires advanced English skills and a detail-oriented mindset. Benefits include opportunities for career growth within a quality-focused team.

Formación

  • Minimum 3 years of experience in process quality within the medical device industry.
  • Experience working in cleanroom environments (ISO Class 7, 8, or equivalent).
  • Strong knowledge of quality tools (PFMEA, 8D, SPC, MSA).
  • Experience in process validation and technical documentation.

Responsabilidades

  • Ensure compliance with ISO 13485 and FDA requirements.
  • Maintain and improve the Quality Management System (QMS).
  • Develop and monitor process controls including statistical analysis.
  • Lead investigations of process-related nonconformities.
  • Support process validations (IQ, OQ, PQ) and revalidations.
  • Conduct risk analysis (PFMEA) and develop control plans.
  • Ensure compliance with cleanroom procedures.

Conocimientos

ISO 13485
Statistical Process Control (SPC)
Process validation
Risk analysis (PFMEA)
Analytical skills
Attention to detail
Continuous improvement mindset
Advanced English

Educación

Bachelor's degree in Engineering

Descripción del empleo

A leading company in the medical device sector in Ciudad Juárez is seeking a Process Quality Engineer to ensure regulatory compliance and process stability in controlled manufacturing environments. The ideal candidate will hold a Bachelor's degree in Engineering and possess at least 3 years of experience in the medical device industry, with strong knowledge of ISO 13485 and quality tools. This role requires advanced English skills and a detail-oriented mindset. Benefits include opportunities for career growth within a quality-focused team.
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