20 beste vacatures voor de functie van regulatory specialist in brussel (nieuwe medewerkers gezocht)

Quality Specialist
Hologic —Zaventem
- € 50.000 - € 70.000 per jaar
- ERP systemen
- Microsoft Office
- Bachelor
Regulatory and Start Up Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Leidinggevende ervaring
- Ter plaatse
Regulatory Affairs Specialist
Hologic —Zaventem
- € 40.000 - € 50.000 per jaar
- Microsoft Powerpoint
- Microsoft Word
- Spaans
12 dagen
Food Ingredient Formulation Scientist
HANDARY —Brussel
- Doctoraat
- Microsoft Office
- Master
Study Start Up Management Specialist - Belgium
IQVIA —Zaventem
- Voltijds
- Thuiswerk
- Onderzoek
- Bachelor
- Ter plaatse
Regulatory Affairs Specialist
Nipro —Mechelen
- Analytisch vermogen
- Bachelor
Senior Specialist Customs Compliance EMEA
Ansell —Brussel
- Voltijds
- Hybride werken
- ERP systemen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Specialist
Nipro Europe Group Companies —Mechelen
- Analytisch vermogen
- Bachelor
Regulatory Affairs Officer
AbbVie —Waver
- Voltijds
- Hybride werken
- Organisatorische vaardigheden
- Communicatieve vaardigheden
EHS Specialist
Medtronic —Brussel
- € 59.200 - € 88.800 per jaar
- Deeltijds
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Internal Audit Manager, Fincrime
Wise Australia Investments —Brussel
- € 5.100 - € 7.750 per maand
Medical Device UniQuality & Unidata Product Information Specialist
MSF International —Brussel
- Deeltijds
- Hybride werken
- Microsoft Excel
- ERP systemen
- Engels
Snel solliciteren
Data Quality Analyst
DHL —Diegem
- Microsoft Powerpoint
- Microsoft Excel
- Engels
1 dag
Global Trade and Tariffs Lead - 1 year contract starting in Sept/Oct 2026
Siemens Healthineers —City of Brussels
- Voltijds
- Hybride werken
- Engels
Key Account Manager Hematology/Oncology (East and West Flanders))
GlaxoSmithKline —Waver
- € 89.250 - € 148.750 per jaar
- Voltijds
- Hybride werken
- Verkoopervaring
- Microsoft Office
Regulatory Affairs - Environment
Nipro —Mechelen
- Hybride werken
- Master
- Bachelor
- ICT
HR International Mobility Officer
Daikin Europe N.V. —Brussel
- Microsoft Excel
- Engels
- Microsoft Office
Belgium : Data Reporting & Visualisation Expert - Freelance (REF18)
Trusted Advisors —Brussel
VP, Head of Clinical Sciences, Vaccines and Infectious Disease
GlaxoSmithKline —Waver
- € 236.250 - € 526.250 per jaar
- Voltijds
- Management
- Doctoraat
- Schrijfvaardigheden
- Pensioensparen
6 dagen
Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT

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Quality Specialist

Hologic -
Zaventem

Nu solliciteren

Vacaturegegevens

€ 50.000 - € 70.000 per jaar

Kwalificaties

Power BI
ERP systemen
Logistiek
Microsoft Office
Bachelor
Productie
Artificiële intelligentie
Onderhandelen

Volledige vacaturetekst

Are you passionate about quality, compliance, and ensuring products reach customers safely and reliably? Do you enjoy working with logistics partners, solving problems, and driving continuous improvement? If so, we have an exciting opportunity for you to join our team as a Quality Specialist, based in Zaventem, Belgium.

This is your chance to contribute to meaningful work in the medical device industry, where your expertise will help ensure our products are stored, handled, transported, and delivered in line with regulatory requirements, Good Distribution Practices, and Hologic’s quality standards.

As Quality Specialist, you will support the assessment, qualification, and ongoing management of Distribution Service Providers, including 3PLs, Logistics Service Providers, and Distributors. Your work will play a key role in maintaining product integrity, supporting compliance, and strengthening our distribution quality processes.

What to Expect:

Assess, qualify, monitor, and requalify Distribution Service Providers in line with regulatory and Hologic requirements.
Maintain lifecycle oversight, including assessments, quality agreements, audits, mitigation plans, corrective actions, and compliance documentation.
Support DSP quality activities, including audits, validation, verification, and Quality System requirements.
Collaborate with Regulatory Affairs and cross-functional teams to confirm local distribution requirements for storage, handling, transportation, traceability, and reporting.
Investigate distribution-related non-conformances and complaints, including product damage and temperature excursions.
Identify root causes and support corrective and preventive actions.
Manage risks across the distribution network and support business continuity where required.
Participate in change control activities related to DSPs, routes, packaging, and storage conditions.
Maintain accurate non-conformance records, SOPs, inspection records, and validation documentation.
Support metrics and KPIs to monitor DSP performance and escalate risks where appropriate.
Identify opportunities to improve Quality System effectiveness in line with ISO 9001, ISO 13485, 21 CFR Parts 11 and 820, and GDP.
Support internal and external audits and cross-functional projects as required.

What We Expect:

Bachelor’s degree in Engineering, Quality Assurance, Supply Chain Management, Logistics, or a related field.
3+ years’ experience in medical device manufacturing or a related regulated industry, preferably within Quality.
Knowledge of Good Distribution Practices, ISO 9001, ISO 13485, EU MDR/IVDR, and medical device regulations.
Experience with root cause analysis, risk assessment, CAPA, and auditing.
Experience with logistics and distribution processes is highly preferred.
Strong communication and stakeholder management skills.
Ability to work independently and collaboratively with internal and external partners.
Good analytical, problem-solving, negotiation, and persuasion skills.
Ability to produce clear reports and define practical action plans.
Proficiency with Microsoft Office tools; Power BI and AI tools are a plus.
Experience with PLM and ERP systems is preferred.
Proactive, organized, adaptable, and able to manage multiple priorities.
Strong ownership, accountability, integrity, and continuous improvement mindset.
Customer-focused approach with a strong commitment to quality.

Why Hologic?

Work on impactful projects that support product quality, compliance, and patient safety.
Partner with internal teams and external providers to strengthen a reliable distribution network.
Grow your career in a supportive, collaborative, and quality-driven environment.
Competitive salary and benefits package, including health insurance.

Travel Requirements: 10% per year
Language Requirements: Proficient in English, written and oral. A second language is a plus.

Salary: €50,000 – €70,000 gross per year

The final offer will depend on experience, skills, and alignment with internal pay structures. In addition, we offer a comprehensive benefits package including pension and insurances.

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regulatory specialist vacatures in brussel

Quality Specialist

Regulatory and Start Up Specialist - Belgium

Regulatory Affairs Specialist

Food Ingredient Formulation Scientist

Study Start Up Management Specialist - Belgium

Regulatory Affairs Specialist

Senior Specialist Customs Compliance EMEA

Regulatory Affairs Specialist

Regulatory Affairs Officer

EHS Specialist

Internal Audit Manager, Fincrime

Medical Device UniQuality & Unidata Product Information Specialist

Data Quality Analyst

Global Trade and Tariffs Lead - 1 year contract starting in Sept/Oct 2026

Key Account Manager Hematology/Oncology (East and West Flanders))

Regulatory Affairs - Environment

HR International Mobility Officer

Belgium : Data Reporting & Visualisation Expert - Freelance (REF18)

VP, Head of Clinical Sciences, Vaccines and Infectious Disease

Regulatory Affairs - Environment

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory specialist in brussel

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