20 beste vacatures voor de functie van regulatory affairs in brussels, bru (nieuwe medewerkers gezocht)

Site Conformance Expert | Life Science
Capgemini Sogeti —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
12 dagen
(Senior) Managing Director - Public Affairs
Burson Global —Brussel
- Hybride werken
- Microsoft Excel
- Engels
- Artificiële intelligentie
Site Conformance Expert | Life Science
Capgemini —Diegem
- € 50.000 per jaar
- Master
- Communicatieve vaardigheden
12 dagen
Director, International Policy Research and Economics
Bristol-Myers Squibb —Eigenbrakel
- Voltijds
- Hybride werken
- Microsoft Excel
- Onderzoek
- Ter plaatse
Stage regulatory affairs
Boiron —Evere
- Microsoft Powerpoint
- Microsoft Excel
- Master
Field Medical Manager
Sandoz —Diegem
- Voltijds
- Communicatieve vaardigheden
Public Policy Manager (all genders) in Brussels
Ridedott —Brussel
- € 50.000 - € 70.000 per jaar
- Voltijds
- Thuiswerk
- Master
- Projectmanagement
- Onderhandelen
Bio DS Operations Quality Manager Weekend
UCB —Eigenbrakel
- Weekendbeschikbaarheid
- Microsoft Powerpoint
- Management
- Engels
Associate Partner - Governance
AION Consulting —Brussel
- Master
- Bedrijfsontwikkeling
Director, EU Public Affairs
Bavarian Nordic —Brussel
- Voltijds
- Verhuiskostenvergoeding
9 dagen
RWE Strategy Lead, Developed Brands (BE)
UCB —Anderlecht
- Doctoraat
- Onderzoek
- Master
Managing Director and Head of Brussels Office
Investment Company Institute —Brussel
- € 200.000 - € 250.000 per jaar
- Engels
- Managementervaring
Snel solliciteren
Compliance Management Expert
skeyes —Steenokkerzeel
- Master
- Analytisch vermogen
- Communicatieve vaardigheden
Legal Advisor
ENTSO-E —Brussel
- Hybride werken
- Onderzoek
- Master
Snel solliciteren
3 dagen
Business Development Manager Africa
Nipro —Mechelen
- Verkoopervaring
- Engels
- Master
Contract Expert Flexibility & Ancillary Services
Elia —Brussel
- Engels
- Secundair Onderwijs
- Ter plaatse
- Pensioensparen
Senior Public Policy Manager (Benelux)
Voi Technology —Brussel
- Hybride werken
- Bachelor
Snel solliciteren
Head of Clinical Standards
UCB —Anderlecht
- Master
- Managementervaring
EU Senior Manager
MEDEF National —Brussel
- Voltijds
- Schrijfvaardigheden
- Organisatorische vaardigheden
Snel solliciteren
Director Switch Technology Coordination (Europe)
Mastercard —Waterloo
- Voltijds
- Communicatieve vaardigheden
13 dagen

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Site Conformance Expert | Life Science

Capgemini Sogeti -
Diegem

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Vacaturegegevens

Vaste Jobs
€ 50.000 per jaar
12 dagen geleden

Kwalificaties

Frans
Master
Kwaliteitsborging
Scheikunde
Communicatieve vaardigheden

Volledige vacaturetekst

Your Role

As a Site Conformance Expert within our Quality Assurance team, you will be the vital link between operations and regulatory affairs, ensuring compliance across multiple production streams including Primary, Secondary, Quality Control, and Incoming Materials.

In this role you will play a key role in:

Ensuring compliance with regulatory dossiers for activities related to Manufacturing Performance Units and Quality Control Departments, through variations and timely responses to health authority questions.
Providing regulatory oversight within Manufacturing Performance Units and Quality Control Departments to maintain consistent alignment with evolving regulatory requirements.
Analysing potential compliance gaps and developing effective mitigation strategies to prevent supply issues, delays, or recalls due to misalignment with regulatory files.
Collaborating with cross-functional teams to implement and maintain quality systems that meet global regulatory standards across all production streams.
Supporting continuous improvement initiatives to enhance compliance processes, documentation systems, and overall quality assurance performance.

Your Profile

We are looking for a motivated and detail-oriented professional who thrives in a regulated environment and is passionate about quality and compliance.

You hold a Master's degree in Pharmaceutical Sciences, Chemistry, Biology, or a related field, and bring a minimum of 3 years of experience in a quality assurance role within the pharmaceutical or life sciences industry.
You have strong knowledge of GMP regulations, quality systems, and regulatory compliance requirements, with hands-on experience in regulatory documentation including eCTD format and normative documents.
You are fluent in both English and French, with strong communication skills that allow you to effectively engage and collaborate with diverse stakeholders across departments.
You are a proactive team player with the ability to manage multiple priorities, work independently, and contribute meaningfully to a high-performing, cross-functional environment.

What you'll love about working here

Career acceleration programs – From associate to leaders and beyond, get support in your career at every stage with award-winning programs such as our leadership development program, Connected Manager, to accelerate your growth and develop your expertise.
Continuous feedback – We take a human-centric approach to foster growth and performance. Our performance management tool GetSuccess enables continuous feedback, quarterly check-ins with managers, and ongoing performance discussions.
FlexAbroad – Employees in 20+ countries can work abroad for up to 45 days in a 12-month period.

For this role, the gross annual starting base salary is 50.000 euro (full-time). This covers base pay only; any bonuses, incentives, and benefits will be discussed later in the recruitment process. Candidates with additional experience or qualifications may receive a higher offer, determined by objective, gender-neutral criteria and consistent with our pay principles. If a collective labour agreement applies, we will explain the relevant pay terms at the interview stage. Note: We never ask for your current or previous salary during our hiring process.

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regulatory affairs vacatures in brussels, bru

Site Conformance Expert | Life Science

(Senior) Managing Director - Public Affairs

Site Conformance Expert | Life Science

Director, International Policy Research and Economics

Stage regulatory affairs

Field Medical Manager

Public Policy Manager (all genders) in Brussels

Bio DS Operations Quality Manager Weekend

Associate Partner - Governance

Director, EU Public Affairs

RWE Strategy Lead, Developed Brands (BE)

Managing Director and Head of Brussels Office

Compliance Management Expert

Legal Advisor

Business Development Manager Africa

Contract Expert Flexibility & Ancillary Services

Senior Public Policy Manager (Benelux)

Head of Clinical Standards

EU Senior Manager

Director Switch Technology Coordination (Europe)

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs in brussels, bru

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