Manager, Regulatory Affairs

Regulatory Affairs Manager EMEAAt NSF International, our mission is to protect and improve human health. We're a global leader in standards development, testing, auditing, certification and training. We provide these services for a diverse set of industries including food, water, health sciences, sustainability and management systems. We're passionate about...

locations- Zaventem- time type- Full time- posted on- Posted Today- job requisition id- JR00010928- For our office in Zaventem, Zoetis is currently looking for a _Regulatory Affairs & Compliance, Associate Manager / Manager._ - JOB PURPOSE: - In collaboration with the RA team members, the RA&C Associate - Mgr / Mgr contributes to the Regulatory day-to-day...

Key responsibilities As a Regulatory Affairs Specialist for our food and food supplement brands you will report to the Regulatory Affairs Manager. Your responsibilities will include, amongst others: - On-time filing of regulatory submissions and post-approval maintenance of regulatory dossiers- Ensure product regulatory compliance for food supplements and...

Key responsibilitiesAs a Regulatory Affairs Specialist for our food and food supplement brands you will report to the Regulatory Affairs Manager.Your responsibilities will include, amongst others:On-time filing of regulatory submissions and post-approval maintenance of regulatory dossiersEnsure product regulatory compliance for food supplements and food with...

USG Professionals is seeking a talented Regulatory Affairs Specialist for a client located in the Zaventem region. This position offers the flexibility to work either as a USG Project Consultant or on a Freelance basis.Job Title: Regulatory Affairs SpecialistCompany: USG ProfessionalsThe Regulatory Affairs Specialist plays a critical role in ensuring...

Are you open to a role as a Regulatory Affairs Project Manager in an international company in medical devices?The Regulatory Affairs Project Manager (RAPM) is responsible for ensuring compliance with regulatory guidelines and successful execution of regulatory submissions. In addition to regulatory expertise, the RAPM integrates project management...

**Job Title**: Regulatory Affairs Specialist **Type**: Junior Role **Time**: 40 hours/week **Location**: Zaventem **Expected Start Date**: Q1 2023 **In this role, you have the opportunity to** Be part of the Business Image Guided Therapy Devices International. You will be able to work in a large and complex organization. Therefore, the job at any level...

Job Title: International Regulatory Affairs SpecialistInternational RA SpecialistPhilips Image Guided Therapy CorporationZaventem, BelgiumIn this role, you have the opportunity to Be recognized as a key talent in international regulatory filings and procedures (excluding USA and Japan). Potential to transition into an internal Subject Matter Expert in a...

Are you open to a role as a Regulatory Affairs Project Manager in an international company in medical devices?The Regulatory Affairs Project Manager (RAPM) is responsible for ensuring compliance with regulatory guidelines and successful execution of regulatory submissions. In addition to regulatory expertise, the RAPM integrates project management principles...

Are you open to a role as a Regulatory Affairs Project Manager in an international company in medical devices?The Regulatory Affairs Project Manager (RAPM) is responsible for ensuring compliance with regulatory guidelines and successful execution of regulatory submissions. In addition to regulatory expertise, the RAPM integrates project management principles...

Contribute to creating a sustainable tomorrow:For many years, climate change has made it clear that we must engage into gradually phasing out fossil fuels. All organizations, especially those in Europe, need an urgent energy revolution given the current geopolitical climate. At TES, we believe that this is an unprecedented moment to tackle both energy...

When our values align, there's no limit to what we can achieve. Are you an experienced regulatory professional looking for a new opportunity? We are currently seeking a talented CMC Regulatory Manager (Regulatory Affairs Consultant) to join our dynamic team This is a client dedicated project, and the role can be office or home based in various...

Job Title: Regulatory Affairs SpecialistType: Junior RoleTime: 40 hours/weekLocation: ZaventemExpected Start Date: Q1 2023In this role, you have the opportunity toBe part of the Business Image Guided Therapy Devices International. You will be able to work in a large and complex organization. Therefore, the job at any level demands knowledge, experience and...

Hello. We're Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we're improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep...

Heb jij aantoonbare ervaring als project manager in Regulatory Affairs en ervaring met medical devices? Voor een bedrijf gelegen te Zaventem zijn we op zoek naar jou!Als Regulatory Affairs Project Manager (RAPM) ben je verantwoordelijk voor het naleven van de richtlijnen en het succesvol uitvoeren van regelgevingsaanvragen. Naast expertise op het gebied van...

locations- Zaventem- time type- Full time- posted on- Posted Today- job requisition id- JR00014179- Zoetis Belgium is looking for a Regulatory Affairs Senior Associate to support the provision of registration dossiers to our in-country regulatory colleagues for submission to national regulatory authorities throughout the Central & Eastern Europe, Africa and...

locations- Zaventem- time type- Full time- posted on- Posted Today- job requisition id- JR Zoetis Belgium is looking for a Regulatory Affairs Senior Associate to support the provision of registration dossiers to our in-country regulatory colleagues for submission to national regulatory authorities throughout the Central & Eastern Europe, Africa and Middle...

About the internship In this role you will take on responsibilities in the Regulatory Affairs team. Your responsibilities will include: - Administrative work, such as document collection and filing - keeping administration up to date, managing document archive- Collaborate with internal and external stakeholders- Interact with project teams and suppliers...

USG Professionals is looking for an Regulatory Affairs Specialist for our client in the region of Zaventem. This can be both as a USG Project Consultant or on a Freelance basis! Functieomschrijving The Regulatory Affairs Specialist is responsible for ensuring compliance with regulatory guidelines and successful execution of regulatory submissions. In...

USG Professionals is looking for an Regulatory Affairs Specialist for our client in the region of Zaventem. This can be both as a USG Project Consultant or on a Freelance basis! Functieomschrijving The Regulatory Affairs Specialist is responsible for ensuring compliance with regulatory guidelines and successful execution of regulatory submissions. In...