Validation Engineer Consultant II

Life Sciences & Health Care - Medical devices - Embedded Software - Academic Bachelor

Looking for an experienced Validation Engineer Consultant to join our client's team in Andover! Our client is a global medical device company, that is looking for someone with 10-15 years of experience to join their team on a part time basis.

Feel free to contact

Daniel Hennelly, Account manager

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About this role

Responsible for driving EU MDR compliance activities, tracking progress and resolving issues with Program Managers for EU MDR compliance for several products;

Other duties include:

  • Establishing processes;
  • Minimizing and mitigating risk;
  • Working with the regulatory staff to complete assessment and administrative procedures.

About you

  • 10-15 years professional experience in a project manager role role. Education: Bachelor's /Master's degree with proven experience;
  • Guide and participate in EU MDR validation, risk assessment, requirement development, protocol and validation report writing;
  • Expertise in software validation for medical devices within manufacturing environment. Ability to learn and adapt to our QMS and work closely our engineering community on new validation methods and re-validation projects.


  • Vacancy number: PUB191698
  • Location: Andover
  • Market: Life Sciences & Health Care
  • hours per week: 20
  • Branche: Medical devices
  • Education level: Academic Bachelor
  • Area of Expertise: Embedded Software
  • Closing date: Thursday, February 7, 2019
Apply now

Feel free to contact


Daniel Hennelly

Account manager Brunel Energy USA Houston

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