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Validation Engineer II

Job description

Validation Engineer II

Responsibilities:

  • Prepare software validation protocols for the Equipment Engineering group.  Execute these protocols and ensure sign-off is obtained at each stage
  • Ensure software is controlled and stored as per validation procedure guidelines
  • Take responsibility for correctly carrying out and maintaining all validation and associated documentation for equipment
  • Provides software validation/compliance guidance and training to staff across various functions as required
  • Develops and enhances cross-functional team relationships and works cross-functionally to identify and resolve technical and organisational issues
  • Ensure best validation practices are employed by the Equipment Engineering Group so as to maximise effectiveness and minimise non-value added work
  • Actively pursues continuous improvement
  • Complete project deliverables and monitor project schedule and scope changes to assure team can meet delivery requirements for related projects
  • Manage all aspects of Equipment & computerised system validation for any software systems used in the manufacture of medical devices.

 

Experience:  

  • Level 8 qualification in Science/Engineering or Quality.
  • Minimum of 5 years’ experience in a Validation role within medical device, biotechnology or pharmaceutical manufacturing organization.
  • Proven track record and performance leading validation teams within manufacturing environment.
  • Availability to travel 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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