Quality Engineer

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What you need to know

An innovative and growing medical devices company in Co. Roscommon who provide their clients with bespoke and high-quality medical device products is currently seeking a Quality Engineer to support the Quality department in maximising production quality performance.

The company provide tailored technical solutions and manufacturing services to an array of leading med-tech companies. They pride themselves on their meticulous and professional approach throughout the manufacturing process and have an outstanding track record of developing new products from concept generation through to commercialisation.

This is a Permanent role with an excellent salary and package.

Your new job

Key duties & responsibilities include:

  • Implement and adhere to the companies Quality Management systems.
  • Review, update and maintain existing quality management processes and procedures.
  • Maintain detailed and accurate quality records, data analysis and documentation.
  • Initiate and drive continuous improvement programs.
  • Lead Quality Engineering activities for the introduction of new production lines and existing product lines.
  • Coordinate process and product validations.
  • Provide quality input to cross functional teams to support existing product lines.
  • Investigate root cause of quality issues and follow through with timely and effective corrective actions.
  • Oversee non-conforming material, customer complaints, CAPA investigations, analysis, and improvement.
  • Conduct internal audits and external audits as required.
  • Mentor and offer support to Junior members of staff on policies and procedures.

What are we looking for?

  • Level 8 or equivalent Degree in Quality Assurance or a relevant discipline.
  • 3 + years’ experience in a Quality Engineering role, preferable in the medical device sector.
  • Strong team player who can work well in multifunctional teams and manage internal and external customers requirements.
  • Proficient with Syspro, Minitab & Lotus Notes, is desirable.
  • Knowledge of ISO 13485, ISO 14971 and QSR 21 CFR Part 820 standards.
  • Strong proficiency in statistical analysis techniques to investigate and solve problems and improve quality.
  • Ability to plan, organise, and prioritise own daily work routine to meet established schedule.
  • Ability to drive projects to completion.

Apply for this job now or get in touch with Oliver at oliver@matrixrecruitment.ie

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    Recruitment Consultant: Oliver Hayes

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