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Part Time Tutor Required within the Medical Device / Pharmaceutical Industry

Job Description

  • Deliver training programmes within medical device/pharmaceutical industries nationwide in the areas of Quality and Regulatory
  • Work within a team to design and develop new training programmes in line with market demands
  • Review existing training programmes and work on improvement projects
  • Correct assessments
  • Complete relevant documentation within a timely fashion
  • General administration work

Requirements

  • Min 5 years experience working within the Medical Device/Pharmaceutical Industry, ideally at a senior/management level
  • Previously worked within Quality/Regulatory Departments with first-hand experience of external 3rd party audits
  • Must have a Training Qualification (minimum certificate level)
  • Min 3 years training experience preferable
  • Must have a good working knowledge of the standard quality/regulatory requirements for these industries
  • Own transport a necessity
  • Must be willing to travel nationwide
  • Attention to detail, good interpersonal and communications skills, Teamwork is paramount

For further information or to apply for this position please send a CV to kevina@micromatters.ie

 

 

 
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CV Available on request

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Kevina O'Donohue is a Member of the TC 209 Working Group involved in updating ISO 14698 Parts 1 & 2 regarding BioContamination Control within Cleanrooms
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