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Regulatory Affairs & Quality Manager

€excellent basic salary plus benefits | Belgium |  Regulatory Affairs, Pharmaceutical Company/Sponsor side |  Permanent  | Ref:890145

The Role

Regulatory Affairs & Quality Manager - Medical Devices - Global Med Devices company - Brussels - £ Excellent basic salary benefits, WFH

The Regulatory Affairs & Quality Manager will be responsible for all regulatory and quality matters for the business. This will include managing a small team of regulatory and quality professionals whilst remaining hands on.


The Company

This is an exciting time to join an expanding, highly successful global medical devices company based at their Belgium affiliate in Brussels. At the forefront of their therapy are, they excel in providing innovative class I-III medical devices across the globe.

  • Leading healthcare company with a presence in 100 countries
  • Established over 50 years ago
  • Proven track record of numerous industry firsts
  • Great career opportunities


The Role

The Regulatory Affairs & Quality Manager will be responsible for managing a small team whilst remaining very much hands on, based in their Belgium affiliate close to Brussels.

  • Manage a complex set of regulatory requirements across the business portfolio within the Benelux region
  • Responsible for regulatory plans, submission, and approval of clinical trial and marketing authorization applications
  • Lifecycle management of marketed products
  • Maintain records of regulatory submissions and communications with the relevant regulatory agencies
  • End to end delivery of product dossiers and technical files
  • Manage a small team



To apply for this role as a Regulatory Affairs & Quality Manager our client is hoping for someone with the following skills and experience;

  • Extensive regulatory experience, currently at Manager level and good experience dossier/technical file creation and registrations
  • Medical Devices regulatory experience
  • Ideally you will come from a pharmacist background before starting your RA career
  • Good level of Dutch (ideally fluent or business fluent)


What should you do next?

This Regulatory Affairs & Quality Manager role is one not to be missed; it encompasses the opportunity to work in a growing healthcare company who are at the forefront of their industry. To discuss further, please submit your current CV.

Unless otherwise stated, if applying for a job within the European Union, you must ensure that you are already authorised to work there.

Carrot Pharma Recruitment Ltd acts as an Employment Business and an Employment Agency on behalf of our client in recruitment for this role.



Hayley Shayestehroo

Which team and area do you work/specialise in?

I work in the Regulatory Affairs team and recruit for Regulatory Affairs professionals at all levels within Pharma, Medical Devices companies and Regulatory Consultancies

What are some of the typical roles you cover?

I cover Regulatory Affairs positions at all levels within Pharma, Medical Devices and Regulatory Consultancies, these typically include;

Regulatory Affairs Associate jobs, Regulatory Affairs Executive jobs, Regulatory Affairs Senior Associate jobs, Regulatory Affairs Manager jobs, Regulatory Affairs Senior Manager jobs, Regulatory Affairs Director jobs, Regulatory Affairs Consultant jobs, Regulatory Writer jobs and Medical Writer jobs.

What are the hot issues in your sector currently?

Within Medical Devices it is the transition from MDD to MDR in May 2020. A lot of medical device companies are hiring Regulatory professionals to prepare their company for the transition

What’s makes you #DistinctlyDifferent?

I take pride in getting to know my candidates on a personal level as well as professional. Changing jobs is a big decision for most people so I like to ensure I am placing my candidates in a role that not only matches their career aspirations but also suits their personal situation and key motivations.


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