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Quality Engineer – North Wales

Quality Engineer – North Wales

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Bond Williams
Professional Recruitment

Quality Engineer required by a medical device manufacturer to support and take ownership for the requirements through the design and development process working closely with internal departments, customers, and suppliers/other companies to understand, plan and execute the design and development stages.

As Quality Engineer responsibilities include:

  • Establish, implement, and promote; quality planning, design control, process control, verification, and validation activities to aid delivery of efficient designs and processes providing safe, effective, and compliant medical devices.
  • Review and approve product and process documentation throughout entire product lifecycle to ensure compliant, effective, and suitably robust design solutions are fully documented.
  • Raise problem reports, non-Conformity report, Corrective Action and Preventive Actions to address product quality concerns and/or QMS concerns.
  • Ensure risk management process is effective and robust in identifying product and process risks and that risk mitigations are implemented to ensure safe and compliant medical devices.

Qualifications / Experience required:

  • Graduate or equivalent calibre in engineering, science, or technology discipline.
  • Experience in a quality related field within a Medical Device design environment or equivalent regulatory controlled environment (product development).
  • Experience in product and process software and hardware V&V.
  • Experience in control of clean rooms for manufacture.
  • Sound understanding of risk management techniques including FMEA.

Be part of something BIG and benefit from working with a progressive company delivering life support devices.

Keywords: Quality; Engineer; Medical Device; QMS; FMEA

Bond Williams Professional Recruitment are an equal opportunity employer and operate as an Employment Business and Recruitment Agency

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