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Sterilization Validation Engineer I

  • Sector: Engineering
  • Contact Email:
  • Job Ref: 22032

Our client a major multinational here in Galway are looking to hire a Sterilization Validation Engineer I, on an initial 17 Month contract.


  • Support routine Sterility Assurance activities e.g GMP, Standards Compliance, Cleanroom Risk Assessment, Limits review, Dose Audit activity, Cycle Requalification, Supplier Change control etc

  • 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 in day-to-day activity, initiating appropriate corrective actions and following through to implementation

  • 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

  • Collaborates with engineering and manufacturing functions to ensure quality standards are in place

  • Devises and implements methods and procedures for inspecting, testing and evaluating the precision and accuracy of products and production equipment.

  • Ensures that corrective measures meet acceptable reliability standards and that documentation is compliant with requirements.

  • Performs calculations, data integrity checks, technical and record keeping duties in conformance with company and regulatory policies and standards to meet quality and accuracy requirements

  • Adhere to all relevant site wide procedures and practices for Safety & GMP


  • Requires broad theoretical job knowledge typically obtained through advanced education. Requires a University Degree, 1-2 years of experience required

  • Excellent communication skills

  • Teamwork skills

For more information and a confidential discussion on the role please contact Michelle Mc Inerney.

091 706 717