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

Regulatory Affairs - Environment
Nipro Europe Group Companies —Mechelen
- Master
- Bachelor
- ICT
Research Scientist II – Extractables & Leachables (E&L) Team Lead
Baxter —Eigenbrakel
- Onderzoek
- Managementervaring
- Communicatieve vaardigheden
- Opleidingsvergoeding CE
Health & Safety Adviser
IMA Europe —Brussel
- Voltijds
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Snel solliciteren
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Local Study Associate Director
IQVIA —Zaventem
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- Master
- Projectmanagement
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Medical Advisor, Cardiovascular (Belgium)
Abacus Medicine —Anderlecht
- Voltijds
- Thuiswerk
- Geneeskunde
- Doctoraat
- Master
11 dagen
Senior REACH Regulatory Compliance Consultant EMEA
The Chemours Company —Mechelen
- € 64.800 - € 140.875 per jaar
- Voltijds
- Hybride werken
- Bachelor
- ICT
- Communicatieve vaardigheden
4 dagen
Transversaal Business Process Owner - Projecten, Strategie & Regulatory Affairs
Belfius —Brussel
- Projectmanagement
- Pensioensparen
12 dagen
Regulatory & Public Affairs Counsel
Eneco —Mechelen
- Hybride werken
- Engels
- Ter plaatse
- Communicatieve vaardigheden
Legal Administrative Assistant
Puratos —Groot-Bijgaarden
- Voltijds
- Microsoft Powerpoint
- Microsoft Word
- Spaans
Head of Regulatory Affairs
Allianz —Brussel
- Voltijds
- Doctoraat
- Engels
- Financiën
Medical Affairs Manager COPD
GlaxoSmithKline —Waver
- € 90.750 - € 151.250 per jaar
- Voltijds
- Geneeskunde
- Communicatieve vaardigheden
13 dagen
Compliance Management Expert
skeyes —Steenokkerzeel
- Master
- Analytisch vermogen
- Communicatieve vaardigheden
Director, International Policy Research and Economics
Bristol-Myers Squibb —Eigenbrakel
- Voltijds
- Hybride werken
- Microsoft Excel
- Onderzoek
- Ter plaatse
Associate Consultant, Tech Policy
APCO Worldwide —Brussel
- Schrijfvaardigheden
- Projectmanagement
- Artificiële intelligentie
Life Sciences Consultant
ALTEN —Brussel
- Voltijds
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- Master
Snel solliciteren
Senior Manager EU Affairs
International Air Transport Association (IATA) —Brussel
- Hybride werken
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4 dagen
Medical Advisor Opthalmology /New Products (M/F/D)
MSD —Brussel
- Voltijds
- Doctoraat
- Verkoopervaring
- Onderzoek
Medical Advisor
Qplus consult —Melsbroek
- Geneeskunde
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- Master
Research Executive - Financial Services
Rud Pedersen Public Affairs Company AB —Brussel
- Financiën
- Master
- Financiële diensten
Funding & Innovation Analyst
Hydrogen Europe —Brussel
- Voltijds
- Microsoft Excel
- Onderzoek
- Master
13 dagen

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Regulatory Affairs - Environment

Nipro Europe Group Companies -
Mechelen

Nu solliciteren

Vacaturegegevens

Kwalificaties

Master
Bachelor
ICT

Volledige vacaturetekst

About the company

As a total solution provider of medical devices and pharmaceutical packaging, Nipro Europe Group Companies (NEGC) is continuously committed to improving patient outcomes and quality of life. We are part of a large global network headed by Nipro Corporation Japan, an industry-leading healthcare company with over 38,000 employees worldwide. Our European headquarters in Mechelen, Belgium covers a wide geographical reach (Europe, Africa, India, the Americas) and is home to Nipro Medical EMEA, Nipro PharmaPackaging International, and the Institute for Medical Practice (iMEP) Belgium.

For Nipro Medical EMEA (NME), we are looking for a Regulatory Affairs Specialist - Environment who is experienced, hands-on, and communicative to join us in ourRAQACA team, based in our EMEA headquarters office in Mechelen, Belgium.

About the role

The Regulatory Affairs Specialist – Environment ensures the compliance of Nipro Medical Europe, its Branch organizations and the products placed on the market by this organization with environmental and sustainability related regulations. This entails Regulatory Intelligence for the EMEA market in the environmental regulatory domain, and operational support for reporting obligations and tender support.

How you will contribute

Operational Support Environment Regulations (40%)

Develop processes to ensure compliance with environmental requirements (REACH, CLP, WEEE, ,...) for the distribution and import of medical devices and biocides manufactured by Nipro factories
Maintaining data and files for future reference, particularly in the event of an audit by a regulatory agency or Nipro Corporation
Act as a liaison between the internal stakeholders at NME, the manufacturer and European agencies to submit required registrations
Collaborate with Nipro customers/distributors related to environmental requests
Support internal tender teams concerning environmental compliance matters
Regularly reporting on compliance status and measures to both internal and external parties

Regulatory Intelligence on environmental Legislation (30%)

Maintain a thorough understanding of new and existing environmental regulations (Substances of Very High Concern, hazardous substances, eco-design, circular economy, packaging, waste) that may impact the organization’s products and processes
Explaining regulations, procedures, and policies to all employees and stakeholders as necessary
Serve as contact point for EU environmental regulatory compliance

Building and Maintaining Knowledge Network within Nipro and with other stakeholders (10%)

Engaging with EU institutions and authorities for the interest of the mother company Nipro Corporation.
Attend task force meetings, working groups and/or events of European organizations on environmental related legislation with the aim to escalate emerging regulatory requirements to the mother company Nipro Corporation
Collaborate with NME HQ, Branches and factories on Environmental topics, e.g. ISO14001, Ecovadis
Collaborate within NEGC ESG team

(Pro-)Active Participation as RAQACA team member (20%)

Contribute to internal projects (e.g. Team Objectives) and activities (e.g. impact assessment of product changes on environmental compliance) of own and other departments
Collaborate with other team members to secure functioning of the RAQACA team

What you bring to Nipro

Bachelor or Master Degree in Regulatory Affairs, Environemental Siences, Life Engineering, Engineering, EU Laws,...
Knowledge of environmental and sustainability regulations (REACH, CLP, WEEE, pakaging, waste management, circular economy and EU sustainability legislation)
Strong analytical and problem-solving skills.
Ability to interpret complex legislation and communicate it clearly.
Experience in regulatory compliance and reporting.
Excellent stakeholder management and collaboration skills.
Strong organisational skills and attention to detail.
Proactive, adaptable and eager to learn.
Team player with a hands-on mindset.

Why you should apply

Make a real impact by helping shape Nipro's environmental compliance and sustainability journey across the EMEA region.
Work at the forefront of evolving environmental and regulatory legislation, influencing how medical devices reach the market.
Collaborate with international colleagues, manufacturing sites, European authorities and industry stakeholders.
Gain exposure to a broad range of topics, including environmental compliance, ESG initiatives, sustainability reporting and regulatory intelligence.
Be part of a purpose-driven company that improves patient outcomes through innovative healthcare solutions.
Enjoy a collaborative and supportive international work environment where your expertise and ideas are valued.

NIPRO delivers on its purpose to help all people Live Longer. Live Better.

Our purpose is grounded in care, respect, and a deep commitment to the well-being of every life we touch—patients, partners, and team members. We believe that every colleague at NIPRO plays a vital role in our mission: to push innovation forward, improve patient outcomes, and make world-class healthcare accessible to all.

Respect is active and essential at NIPRO - it is our way of working, thinking, and growing together. We promote an environment where people feel safe to contribute, constructive ideas flow freely, and every person is treated with dignity.

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regulatory affairs vacatures in diegem, vlg

Regulatory Affairs - Environment

Research Scientist II – Extractables & Leachables (E&L) Team Lead

Health & Safety Adviser

Local Study Associate Director

Medical Advisor, Cardiovascular (Belgium)

Senior REACH Regulatory Compliance Consultant EMEA

Transversaal Business Process Owner - Projecten, Strategie & Regulatory Affairs

Regulatory & Public Affairs Counsel

Legal Administrative Assistant

Head of Regulatory Affairs

Medical Affairs Manager COPD

Compliance Management Expert

Director, International Policy Research and Economics

Associate Consultant, Tech Policy

Life Sciences Consultant

Senior Manager EU Affairs

Medical Advisor Opthalmology /New Products (M/F/D)

Medical Advisor

Research Executive - Financial Services

Funding & Innovation Analyst

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van regulatory affairs in diegem, vlg

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