RA Intelligence Officer – Open to graduates

Location:

Leuven – Flemish Brabant, Flanders, Belgium

Salary:

€3300 – €5000 per month + meal vouchers, insurances,…

Type:

Permanent

Main Industry:

Search Health, Nursing & Social Services Jobs

Advertiser:

NonStop Consulting

Job ID:

133139778

Posted On:

30 June 2026

Our client, a leading global medical device manufacturer, is offering an exceptional entry point into regulatory affairs. This role is open to junior graduates, giving you the chance to step directly into the industry and build practical expertise in Regulatory Affairs. From day one, you’ll gain hands-on experience monitoring legislation and standards across Europe, the US, Canada, Australia, Taiwan, China and other key markets, all within a supportive, knowledge-rich RA department.

Benefits

* Career-defining entry role: Ideal for junior graduates wanting to break into regulatory affairs and develop strong, practical skills.
* Big multinational company: Career opportunities internally, a lot of people progress within the company and there is very good retention which gives you a good long-term career vision.
* Strategic international scope: Build deep expertise in European and global regulations and standards while supporting compliance and market access across EMEA and beyond.

Role Responsibilities

* Monitor and analyse regulations & standards: Support the tracking and interpretation of medical device legislation and standards (ISO/EN/IEC and national) across Europe and key global markets, feeding into CE marking, registrations and tender activities.
* Maintain regulatory intelligence tools: Help maintain key reference lists and contribute to the internal regulatory database, supporting impact analyses and the implementation of new and revised standards.
* Support organisation-wide compliance & training: Assist the RA Director and RA Intelligence Specialist with monthly regulatory reporting, training sessions and interactions with external working groups to align regulatory intelligence with the company’s mission of safe, compliant patient care.

Requirements

* Master Degree in Science (Biomedical Sciences, Pharmaceutical Sciences,…)
* Several years or internship experience in regulatory affairs is a plus, but not required
* Interest in global regulations & standards
* Strong analytical, communication and organisational skills
* Fluent level of English

If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Consulting website or on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.

Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.

About NonStop: We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We’re passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting (nonstopconsulting), for more information, to browse all our roles, or to let us know how we can help you.

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