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Design Quality Assurance Engineer (DQA)

Establishment Labs · Coyol

Nuevo
Hybrid Mid 🇬🇧 English
FDA QMSR EU MDR ISO 13485 ISO 14971 ISO 62366 IEC 60601

Descripcion del puesto

About the role

Establishment Labs designs, develops and manufactures medical aesthetic devices and wellness solutions, with production in Costa Rica. As a Design Quality Assurance (DQA) Engineer you represent the quality perspective across the medical device product lifecycle, from new product development to design changes and sustaining activities. You partner with R&D, Regulatory Affairs, Clinical Affairs, Manufacturing and other teams to support design controls, risk management, usability engineering and regulatory compliance.

Key responsibilities

  • Provide quality and compliance input to new product introduction projects, design changes, supplier and process changes.
  • Support design controls: planning, user needs, inputs and outputs, design reviews, design V&V and design transfer in an FDA/EU MDR environment.
  • Lead design validation and usability engineering activities, including strategy, formative and summative evaluations, and their records and reports.
  • Maintain product risk management documentation such as hazard analyses, FMEAs, risk management files and reports.
  • Review and approve engineering documents and design control deliverables such as specifications, test methods, protocols and drawings.
  • Support investigations of nonconformances, CAPAs and risk-based impact assessments.
  • Partner with Regulatory Affairs on annual reviews, recertifications and registration responses.
  • Support internal and external audits and champion compliance with policies, work instructions and SOPs.

Required profile

  • Bachelor's degree in Industrial, Industrial Production, Biomedical, Mechanical, Chemical, Materials, Electrical or Electronic Engineering.
  • At least 2 years of experience in a medical industry quality department as an engineer.
  • Advanced English (B2+).
  • Self-motivated, able to manage multiple priorities, detail-oriented, flexible and strong communicator.

Required skills

  • Knowledge of FDA QMSR, EU MDR, ISO 13485, ISO 14971, ISO 62366 and IEC 60601.
  • Validation and statistical techniques.

The schedule is Monday to Friday, 8:00 a.m. to 5:00 p.m., in a hybrid role. Selection involves a test to the process, an English assessment, an assessment center evaluation and a competency-based interview with the hiring manager and team.

Questions fréquentes

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Publicado hace 6 horas

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Establishment Labs

Coyol