Job Detail

Location Mayo
Salary Negotiable
Posted
Role Type Permanent
Contact Clara Burke
email science@hero.ie

Validation Supervisor

Validation Supervisor
A leading medical device company in Mayo is looking to hire a Validation Supervisor for their site on a permanent basis.
You’ll be working on developing and implementing Master Validation Plans and lead QE activities in the Value Stream.

Responsibilities:

  • Develop Master Validation Plans
  • Develop and complete DV/IQ/OQ/PQ protocols
  • Develop product specifications / drawings / quality plans in conjunction with NPD personnel
  • Provide QE support for NPD projects
  • Process Risk Management / FMEA
  • Complete internal audits per the audit schedule
  • Co-ordinate and implement process capability analysis on catheter processes
  • Complete CAPA investigation
  • Lead Quality Engineering team

Experience and Qualification:

  • 10 years experience in Medical Device Industry utilizing automated equipment
  • Experience of people management
  • Degree in Engineering/Science Discipline and Quality Engineering Qualification.
  • Experience in statistical analysis / SPC / validation of automated equipment

For further information on this Validation Supervisor role in Mayo please contact Clara Burke on 086-8168273/ science@hero.ie

Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/
Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval.

109880

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Validation Supervisor

Clara Burke

Role Type Permanent
Contact Clara Burke
email science@hero.ie
mobile +353 86 816 82 73
linkedIn profile click here

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