RA Specialist

Ede, The Netherlands

RA Specialist
Ede, The Netherlands
Regulatory Affairs

Your Role
In a team of 8 people, you will fulfill a position of RA Specialist. It will be your challenge, together with the QA/RA team, to deliver top performance as demanded by regulations and customers.
As Regulatory Affairs Specialist you are in close contact with OEM manufacturers, local distributors and competent authorities worldwide. You will develop registration strategies, register new In-Vitro Diagnostic medical devices and support OEM manufacturers and local distributors with registrations.
Your Profile

  • Higher education or academic degree
  • Enthusiastic, highly motivated, self-disciplined and well-organized
  • Results oriented and eager to learn
  • Customer-focused and process-oriented
  • Strong oral and written communication skills in English and Dutch
  • Preferably knowledge of compliance requirements and quality guidelines
  • Preferably relevant work experience (1-3 years)

Why should you apply?

  • A position in a healthy organization with a promising future
  • Personal development through guidance, education and knowledge sharing
  • A competence development model focused on your personal ambitions
  • Support in creating safer healthcare
  • Able to leave your mark on the job
  • A market-competitive salary and dynamic work environment

The Company
Eurotrol is an international company that provides high specification, custom-made quality control materials for in vitro diagnostics. For more information about the company or the job visit our website at www.eurotrol.com