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Quality Engineer II, CR (Shift C)

Terumo Neuro · Alajuela

New
Mid 🇬🇧 English
PFMEA CAPA FMEA Root cause analysis ISO 13485 MS Office Minitab DOE

Job description

About the role

Terumo Neuro is hiring a Quality Engineer II (Shift C) in Alajuela, Costa Rica, to support the development and manufacturing of existing and new medical devices. The engineer works with Manufacturing and R&D to resolve product quality issues, including field complaints, and supports manufacturing process changes, product design improvements and the introduction of new products.

Key responsibilities

  • Review process changes with manufacturing engineers, resolve quality issues and assess related risks.
  • Work with suppliers to maintain high quality of incoming materials and take part in supplier quality audits when required.
  • Support new product implementation with R&D by reviewing quality and testing plans, and help develop FMEAs.
  • Develop test protocols and reports (design verification, design validation, process qualification and validation) and review their execution.
  • Maintain quality systems such as CAPA, non-conformance, supplier quality, equipment calibration, internal auditing and quality metrics data analysis, as assigned.
  • Comply with laws and regulations, follow Quality Management System processes and act with ethics and integrity.

Required profile

  • Bachelor's degree in engineering or a related field.
  • At least 3 years of related medical device manufacturing experience.
  • Intermediate computer skills and knowledge of MS Office (Word, Excel, PowerPoint, Teams, Outlook).
  • English level B1 or above (based on the Belt Certification Process).
  • Ability to read and interpret PFMEA risk assessments, validation processes (TMs/VQPs, VQRs) and production controls, and to handle nonconforming products.
  • Minimum 1 year of root cause analysis experience (Fishbone) and 1 year of firsthand experience with nonconforming product handling.
  • Strong written and verbal communication skills.

Required skills

  • Desired: basic knowledge of ISO 13485 and familiarity with medical device quality systems and complaint handling.
  • Desired: statistical software (Minitab, Stratigraphic, DOE).
  • Desired: basic knowledge of risk management (e.g., ISO 14971).

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Published 7 hours ago

Expires 1 month from now

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Terumo Neuro

Alajuela