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Regulatory Affairs Specialist – near Brussels – negotiable salaries.

Option-to-start-immediately28+-day-annual-leaveAnnual-performance-bonusBonus-schemeHybrid-working

The Company

As a Regulatory Affairs Specialist at our client's Benelux facility, you will ensure that products comply with Benelux legislation. Collaborate with teams on launch campaigns, material review, document changes, and regulatory compliance. A critical function in ensuring that products fulfil regulatory marketing and sales compliance requirements. Join a diverse and inclusive environment.

Our client is a global leader in medical technology, dedicated to improving health throughout the world. With billions of MedTech products made each year, our mission is to turn the impossible into realities through inspiration and enthusiasm in all elements of our operations, from design and engineering to production and marketing.

The Role

  • Answering questions from customers

  • Supporting customer service for tenders

  • Assisting cross-functional teams with product launches

  • Reviewing promotional materials in both French and Dutch

  • Updating regulatory documents and internal databases

  • Keeping track of regulatory changes in Benelux

  • Attending internal meetings with the EU Regulatory Affairs team or project teams

  • Participating in trade associations and supporting regulatory activities for various product categories are just a few of the responsibilities that come with being a regulatory affairs specialist.

You

  • Master degree in sciences or pharmacy or equivalent

  • Previous experience in regulatory affairs of 1 year at least ideally in medical devices or in vitro diagnostics area

  • Good communication skills verbal and written in Dutch and English (French is nice to have)

  • Ability to handle several projects in parallel and interact with several functions

  • Computer skills including the office pack

Even if you don’t think you match the requirements above, still get in touch with me to discuss your career options. These requirements are a guide only with certain elements being more flexible than others and we would be happy to discuss this with you.

What should you do next?

This Regulatory Affairs Specialist role is one not to be missed; it encompasses the opportunity to work with a fantastic company. To discuss this role further or to find out about other roles I’m currently working on, please get in touch or hit apply to submit your current CV.

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

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

We are an Equal Opportunity Employer and do not discriminate against any employee or applicant for employment because of race, colour, sex, age, national origin, religion, sexual orientation, gender identity and/or expression.

If there are any arrangements or adjustments we can make to assist you at interview then please let us know and we'll be more than happy to assist.

 

Apply Now!

Job Consultant

Enzo Bagmanian

Regulatory, Quality & PV

Recruitment Consultant

enzo@carrotrecruitment.com

+44 (0) 2393 874 292

 

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