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  • Location

    Leiden, Netherlands

  • Job title:

    Project Manager EU MDR

  • Sector:

    Medical Devices

  • Job ref:

    43358

The company

Our client is a Medical Device company located in Leiden, Zuid-Holland. They are a leading supplier of medical products for the global aesthetic medicine market.

Role description

You will guide the process with notified body (grant the EU / FDA certification) and lead the implementation of the new Medical Devices regulations EU MDR projects.

Responsibilities

  • Manage the implementation of regulations within EU-MDR projects

  • For the shaping and defining of the implementation you will work closely with experts on EU MDR regulation

  • Reporting progress and responsible for stakeholder management

  • Map required EU MDR deliverables and plan for 2020 and beyond

  • CSS Plant Site MIP owner

Requirements

  • 5+ years of experience as a Project Manager

  • Experience with Project Management within a regulated environment like Medical Devices or Pharma (or other highly regulated industry)

  • Fluent in English (oral and written), Dutch is a plus

  • Engineering background would be a plus


This is a fulltime job, 32 hours is discussable. An experienced Project Manager is what our client is looking for, EU MDR expertise is not needed. You must be able to be on-site at least 80% of working hours (min. 3-4 days a week).

Interested in this job? Click on 'Apply now' below.

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