20 beste vacatures voor de functie van regulatory affairs in groot bijgaarden (nieuwe medewerkers gezocht)

Clinical Affairs Officer
Covartim —Brussel
- € 2.800 - € 5.500 per maand
- Engels
Regulatory Affairs Specialist
Hologic —Zaventem
- € 40.000 - € 50.000 per jaar
- Microsoft Powerpoint
- Microsoft Word
- Spaans
Medical Information & PV Officer
Chiesi Farmaceutici —Zaventem
- Bachelor
- Communicatieve vaardigheden
- Verpleegkunde
Government Affairs: Internship Opportunities
Microsoft —Brussel
- € 2.200 per maand
- Projectmanagement
- Stage
- Communicatieve vaardigheden
5 dagen
Junior Regulatory Affairs Advisor
PwC —Brussel
- Voltijds
- Hybride werken
- Engels
- Master
- Bachelor
14 dagen
REGULATORY AFFAIRS INTERNS - OBELIS SCHOOL OCTOBER 2026
Obelis Group —Brussel
- Microsoft Office
- Master
- Bachelor
Policy Officer – LE5 – DISR – Brussels
The Commonwealth Government of Australia —Brussel
- € 5.922,26 per maand
- Voltijds
- Microsoft Office
- Analytisch vermogen
- Personeelszaken
1 dag
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Auditor QA Pharmaco Vigilance | Brussel | 4 days/week
Plasma Industries Belgium —Brussel
- Microsoft Excel
- Microsoft Access
- Bachelor
Legal Administrative Assistant
Puratos —Groot-Bijgaarden
- Microsoft Powerpoint
- Microsoft Word
- Spaans
EU Public Affairs Consultant
Milltown Partners —Brussel
- € 60.000 - € 70.000 per jaar
- Voltijds
- Projectmanagement
- Artificiële intelligentie
- Communicatieve vaardigheden
Government Affairs and Public Policy Analyst
Google —Brussel
- € 80.000 - € 82.000 per jaar
- Doctoraat
- Master
- Bachelor
8 dagen
Regulatory Affairs - Environment
Nipro —Mechelen
- Hybride werken
- Master
- Bachelor
- ICT
Human Resources Intern, Public Affairs Consultancy, 6-month paid internship
FleishmanHillard —Brussel
- Microsoft Excel
- Microsoft Office
- Personeelszaken
- Taalopleiding voorzien
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Senior Clinical Research Associate
BD —Erembodegem
- € 60.300 - € 91.950 per jaar
- Onderzoek
- Projectmanagement
- Bachelor
8 dagen
INTERNSHIP - Based in Brussels
Flint Global —Brussel
- Voltijds
- Hybride werken
- Onderzoek
- Projectmanagement
- Organisatorische vaardigheden
Snel solliciteren
6 dagen
Regulatory Affairs advisor
Elia —Brussel
- Master
- Communicatieve vaardigheden
5 dagen
Drug Safety Advisor
Qplus consult —Melsbroek
- Doctoraat
- Master
Communications and Patients Engagement Officer VIE Contract
Sanofi —Diegem
- Marketing
- Master
- SharePoint
6 dagen

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Clinical Affairs Officer

Covartim
Brussel

Nu solliciteren

Vacaturegegevens

€ 2.800 - € 5.500 per maand

Extralegale voordelen

Elektronische maaltijdcheques

Kwalificaties

Frans
Engels
Nederlands

Volledige vacaturetekst

A validator of innovative medical technologies

You want to make use of your medical expertise?

CIP, CIR, CEP, CER, PMS, PMCF, PSUR ring a bell for you?

Do you agree that the matter lies in the details or beyond the details?

Then you cannot miss this job ad!

Who we are?

COVARTIM is an engineering company. Our mission is to help the MedTech industry foster medical innovation and improve health care.

More concrete we support any kind of organisation (practitioners, startups, SMEs, big companies) in the development and the certification of their medical technologies.

In a nutshell:

Launched in 2016 by Kyun, Founder and Director, passionate about medical technologies and working in the field for more than 15 years;
A (small) team of 15 people (24-52 years old) always ready to help each other (and play table football);
6 managers leading the team but also working on the projects: Aurore, Isabelle, Arnaud, Laurent, Hervé and Kyun;
40+ projects in parallel every month;
150+ clients in BeNeLux, France, USA, Japan, Finland, …

In order to answer the constantly growing demand from current and future clients, we are looking for a Clinical Affairs Officer.

The job is located in Brussels or Liège for an open-ended period, to be filled immediately.

Ready ?

Practically, what will you do?

Prepare and manage submission for clinical investigations in EU and US;
Prepare CEP and CER;
Perform state of the art research and analysis;
Set up and follow up PMS, PMCF, PSUR;
Review and prepare documentation packages for notified bodies, FDA, competent authorities.

How ?

We perform projects for our clients in our office in Brussels and in Liège. We go to our clients' premises for kick-off and follow-up meetings and for audits. Some clients want to see us once a week, others are located at thousands km from Brussels and only see us on Teams. This means that we spend most of our time at the office, together with the team.

What about the team ?

Our members are gathered in two teams : the Development team and the Quality Assurance & Regulatory Affairs (QA/RA) team. As a Clinical Affairs Officer, you will join the QA/RA team that includes 6 people and that is led by Aurore.

The mission of the QA/RA team is to help our clients achieve the compliance of their devices with regards to the regulatory framework and to provide support for the introduction on the market.

Examples of projects:

Management of clinical investigation submission for a wearable diagnostic device (Class IIb);

Management of clinical investigation submission for a xenograft scaffold (Class III);

Review and update of CEP/CER for endoscopic tools (Class IIa, IIb);

Update of CEP/CER of IVD systems, including reagents (Class C).

In order to fulfill your mission, you will need:

A good understanding of Medical Devices and IVD regulatory environment (directives, regulations);
A good knowledge of medical devices clinical investigation clearance process (EU and US);
A good knowledge of medical devices risk management, CIP, CIR, CEP, CER, PMS, PMCF, PSUR;
A solid scientific background;
A good knowledge of literature search review;
To speak English and French/Dutch to communicate with our clients and our cosmopolitan team;
To make clients' satisfaction a priority by combining quality and professionalism;
Driving license.

Every seniority level is welcome!

You start your career? Our team will be there to guide you! You will collaborate on several projects and you will quickly have an overview of what can be done here. Cherry on top: you will learn and discover a lot in a short time!

You have got a first experience already? We will support you in the development and the enhancement of your knowledge and know-how. You will become more and more autonomous, take the lead on your projects and coordinate team work.

You have got a proven experience? We will be happy to make our clients and colleagues benefit from your expertise! You will get introduced to our methods then you will take the full lead on challenging projects.

But what if you want to develop your skills and grow within COVARTIM?

Once a year you will define your goals with your manager. It will be a good opportunity to discuss your expectations and needs in terms of responsabilities and training as well as your salary. After 6 months your manager will make sure that you are on the right track to achieve your targets and that your expectations have not changed. Based on the level of your autonomy, your control and your skills you will have the chance to grow within your team and/or the company itself.

Homeworking

We know that homeworking is a must nowadays. However when several people work on the same project the office remains the best option for interactions, ideas and pieces of advice sharing. Same for the coaching which is essential during the first months.

Once you have become more autonomous you will apply for one or two days per week at home.

Our offer

Salary range and other benefits:

Based on your skills and seniority, you can expect a monthly gross salary within 2.800 euros and 5.500 euros.

In addition you will get meal vouchers (8 euros/day), a supplemental health insurance (DKV Belgium) and a complementary pension.

Public transport costs are fully covered and you will get compensated for the usage of your own car.

In addition to 20 legal days off, you will get 2 extra days and up to 5 seniority days.

Training:

On your arrival and all along your career at COVARTIM you will get many opportunities of learning (technical topics and soft skills).

Well-being at work:

At COVARTIM we care of our members' well-being:

Attentive director and managers;
Weekly monitoring of mood and feelings;
A comfortable, spacious and colorful office surrounded by greenery;
A good balance between work and life;
Activities that strengthen group cohesion and make the atmosphere even more pleasant (after-works, team-buidings, table football, sport sessions, …);
And cherry on top: one well-being workshop per quarter (yoga class, nordic walk, seated massage, cooking class, ...).

Apply

Get to know us better and apply on Welcome to the Jungle :

Or send your application and resume to

Kyun Thibaut
Managing Director
[email protected]

Nu solliciteren

Verfijn je zoekopdracht

regulatory affairs vacatures in groot bijgaarden

Clinical Affairs Officer

Regulatory Affairs Specialist

Medical Information & PV Officer

Government Affairs: Internship Opportunities

Junior Regulatory Affairs Advisor

REGULATORY AFFAIRS INTERNS - OBELIS SCHOOL OCTOBER 2026

Policy Officer – LE5 – DISR – Brussels

Regulatory Affairs Specialist

Auditor QA Pharmaco Vigilance | Brussel | 4 days/week

Legal Administrative Assistant

EU Public Affairs Consultant

Government Affairs and Public Policy Analyst

Regulatory Affairs - Environment

Human Resources Intern, Public Affairs Consultancy, 6-month paid internship

Regulatory Affairs Specialist

Senior Clinical Research Associate

INTERNSHIP - Based in Brussels

Regulatory Affairs advisor

Drug Safety Advisor

Communications and Patients Engagement Officer VIE Contract

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs in groot bijgaarden

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