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

Apply now

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.

Summary

  • 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

DH

Daniel Hennelly

Account manager Brunel Energy USA Houston

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