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Quality Systems Engineer

Job Title: Quality Systems Engineer
Contract Type: Permanent
Location: Limerick
Industry:
REF: 122333
Job Published: over 1 year ago

Job Description

Quality Systems Engineer:

Our client a leading Multinational Healthcare company now require a Quality Systems Engineer.

The Quality Systems Engineer will maintain the Internal Audit System and act as Quality Auditor. The responsible person will also assist in the implementation and improvement of all aspects of the quality management system (QMS).

This is a permanent role based in Munster.

Responsibilities for Quality Systems Engineer:

  • Maintain the Internal Audit System as the Quality Auditor with a team of Internal Auditors
  • Conduct in-depth Internal Audits of all aspects of the QMS against the relevant regulations
  • Detailed knowledge of the Medical Device regulations, guidance and requirements.
  • Ability to implement and improve a QMS
  • Organise and manage site preparation for Regulatory and Corporate Audits
  • Manage Audit back rooms for Regulatory and Corporate Audits
  • Provide Quality Systems support to all areas of the QMS, ensuring compliance is maintained at all times
  • Conduct Supplier audits
  • Ability to lead and drive assigned Process Improvements essential
  • Prepare, implement and analyse key Quality Systems related documentation
  • Provide input and support to the company Corrective and Preventive Action (CAPA) program
  • Provide training on the Quality Manual and other key Quality Systems procedures
  • Prepare Management Review presentations as appropriate
  • Provide meaningful Quality measurement while ensuring that in-house or external Quality issues are effectively prioritised and acted upon in a timely manner
  • Provide inputs to KPI?s and Management Review

Requirements for Quality Systems Engineer:

  • Third Level Qualification in Quality, Science or Engineering
  • Proven knowledge and experience (min 4 years) of working with ISO13485:2003, ISO14971: 2000, the Medical Device Directive and the FDA QSR including 21 CFR Part 820 and 21 CFR Part 11, ideally gained in the medical device industry
  • Desired is a qualified and experienced Lead Auditor, preferably within the Medical Device Industry
  • Strong interpersonal skills with the ability to communicate effectively at all organisational levels

For more information please contact John at The RFT Group on 01 2302400/ www.rftgroup.ie

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The RFT Group, BioPharmaceutical Division specialise exclusively in the recruitment of scientists, engineers and executives for the biotechnology, pharmaceutical and medical device sectors.