Senior Regulatory Affairs Specialist
Limburg, Belgium
9 dagen geleden

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation.

We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies.

By using highly advanced algorithms, we enable our team of Resource & Data Strategists to maintain the most advanced, detailed and complete Life Sciences network in Europe.

This big data enables us to work Reverse Recruitment : we first analyze the market in-depth before we go out to the market.

Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment , making sure we, or better yet, you find the right career!Our client is a professional Medical Devices organisation, based in Limburg Belgium.

The Company

This organisation has an extensive portfolio of Medical Devices. Their products vary from endoscopy to interventional oncology.

They are internationally represented and currently experience a growth for their EMEA site.

Role Description

In your role as Regulatory Affairs specialist, you will gain the responsibility to collect, maintain and adjust technical files and relevant documentation.

You will have a supportive role in creating awareness and exchange of knowledge about international regulations and changes.

In addition, you interact with internal and external stakeholders and you will ensure that they are provided with the required information.

Next to that, you are involved in the development of strategic plans which are related to the Regulatory Affairs and the implementation.

This project is set for a year and can possibly be extended.


  • Key contact person concerning Regulatory Affairs for internal and external stakeholders among which authorities and notified bodies
  • Creating awareness and spread of knowledge regarding RA related topics and procedures
  • Supportive and advisory role as team lead, and for subsidiaries of the organisation
  • Overviewing the ongoing changes and points of improvement for the Quality Management System and relevant, required documentation
  • Maintenance and controlling of the required regulation standards and legislation
  • Follow up on the latest developments for Medical Device regulation and creating strategies to apply these regulations
  • Development of trainings and exchange of knowledge across teams and other departments
  • Leader during internal and external audits from the beginning to the end of the process, and making reports of these audits
  • Requirements

  • Bachelor in Life Sciences
  • Minimal 6 years of experience in the Medical Devices sector
  • Minimal 4 years of experience in a RA role
  • Excellent knowledge of the Medical Device Directive, and preferably the MDR
  • Experience with regulations and submissions of EMEA countries, preferably Eastern Europe, Middle-East or North-Africa
  • Experience with products varying from class I to III
  • Excellent writing and verbal skills in English
  • Knowledge of the ISO 13485, particularly the 2016 norm
  • Strong analytical skills and eye for detail
  • Team player, yet individual operator
  • Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.

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