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Sterilisation Validation Engineer

Job description

This is an 18 month contract. 

What you will do:

  • Support sterility assurance activities for new products and change control, developing strong partnering relationships with these groups, at both manufacturing and design sites
  • Participate in root cause investigations and continuous improvement projects, initiating appropriate corrective actions and following through to implementation
  • Support a MDR project work for Sterilisation Validation team
  • Support cross functional teams in design protocols to ensure that new products/ product changes are adequately evaluated/tested to guarantee compliance to all regulatory standards

What you will need:

  • Bachelors’ Degree (Level 8) in Science/Engineering or related Discipline
  • 2 years’ experience with Sterilisation Validation or Biocompatibility is desirable

What you will receive:

  • Competitive Salary & Comprehensive Benefits Package, Training & Development

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