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Validation Engineer

Job description

Validation Engineer

You will manage all aspects of Equipment & Computerized system validation for any software systems used in the manufacture of medical devices.
 
Responsibilities:

  • Prepare software validation protocols for the Equipment Engineering group.  Execute these protocols and ensure sign-off is obtained at each stage.
  • Work with Quality department to ensure equipment validations are in line with global and site validation standards.
  • Take responsibility for correctly carrying out and maintaining all validation and associated documentation for equipment.
  • Ensure best validation practices are employed by the Equipment Engineering Group so as to maximize effectiveness and minimize non-value added work.
  • Project management of sustaining projects
  • Actively pursues continuous improvement
  • Generates quotations for new and upgrade software systems.

 

Experience:

  • Level 8 qualification in Science/Engineering or Quality.
  • Minimum of 3 years’ experience in a Validation role within medical device, biotechnology or pharmaceutical manufacturing organization.
  • Proven track record and performance executing validation activity independently or as part of a team in multiple areas.
  • Availability to travel as required.
  • Ability to support weekend work as required

 

To apply for this position please contact Catherina at Sigmar Recruitment T: +353 91 749261 E:  cforde@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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