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Senior Quality Engineer

Job description

Responsibilities

  • Possesses and applies comprehensive knowledge of Quality and QMS while being able to deliver in QA projects and help with the core development of Quality Procedures.
  • Drive compliance across the site and work cross functionally with other sites to develop alignment for ISO13485 certification.
  • Independently performs assignments with instruction limited to results expected.  Determines and develops approach to solutions.
  • Drive business imrovement by taking charge of projects and mentoring junior staff and helping them to develop.
  • Drives business improvements through mentoring and support for the continuous improvement initiatives while also being part of Audit team
  • Escalation point for quality related non-conformances and CAPAs

Requirements

  • Third level qualification in Quality Engineering or similar
  • Minimum 5 years of experience in medical device industry with good knowledge of Quality Management Systems (e.g. ISO9001/ ISO13485/ ISO14971/ GMP) and Awareness of relevant laws and regulations (e.g. CE/ FDA/ PAL)

 

To apply for this position please contact James Porter at Sigmar Recruitment T: +353 91 455305 E:   jporter@sigmar.ie  

All applications will be treated with the strictest of confidence.  Sigmar will never forward your CV to a third party without prior consent

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