Eu Regulatory Affairs Advisor

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...

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...

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...

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...

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...

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...

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...

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...

Who you areWe are looking for an experienced EU Public Affairs Leader to join our team within Ingka Group Public Affairs and Advocacy. You will work with us on our exciting EU topics and be a key partner to our global PA team as well as country teams in our many IKEA markets.Who you are.You are passionate about working with and influencing EU policymakers,...

locations Zaventem time type Full time posted on Posted Today job requisition id JR Zoetis is currently looking for a Senior Associate Regulatory Intelligence. POSITION RESPONSIBILITIES: A Senior Associate on the Regulatory Intelligence Team will be responsible for supporting the management of global evolving regulations within Global Regulatory Affairs at...

Overview:We are recruiting Director Government Affairs EU & DACH to help create EU and German regulatory environments that allow responsible FMCG companies to flourish sustainably.Responsibilities: Monitor, report and help shape legislative and regulatory developments in the EU and Germany Provide regular policy updates and briefings on EU and German policy...

**Vacatureomschrijving**:Ter versterking van ons team zijn we op zoek naar een specialist vergunningen en regelgeving. Kun je zeer georganiseerd werken en heb je oog voor detail? Solliciteer dan vandaag nog. In deze functie ben je verantwoordelijk voor het beheren en verkrijgen van vergunningen voor diverse projecten. Je hebt dan ook de vaardigheden om...

Position description Job title (Sr) Advisor Internal Audit (Risk & Regulatory) Function Advisory - Senior Advisor Roles & Responsibilities A corporate culture in which personal growth, mutual trust and lifelong learning are being fostered. An inclusive workspace that encourages diversity and pursues mutual respect for each other's beliefs and...

This job in a nutshell:We are currently searching for an experienced senior manager to further build the Compliance business unit for Banking. As the Compliance Senior manager, you will help drive the compliance agenda forward and you will play an important role driving the change at Banks. You have extensive experience in the implementation of new rules &...

We are seeking a Compliance Expert for Social & Governance matters to join our Service, Quality and Environment function. You will take the lead with legal tracking, interpretation and concluding on vital actions with regards to the new and updated legislation affecting Sony operations and products. As a representative of Sony at trade associations, you'll...

**Qplus consult is op zoek naar een Case Management Associate**:Qplus consult biedt hoogwaardige diensten voor farmaceutische bedrijven. Binnen de farmaceutische sector heeft Qplus Consult een solide en sterke reputatie opgebouwd, daarom zijn we op zoek naar een gemotiveerde, dynamische en **Case Management Associate** om ons team te versterken.**Wat is de...

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to...

Qplus is looking for a Medical Writer:Qplus consult offers high-level quality services for pharmaceutical companies. Within the pharmaceutical sector Qplus consult built a solid and strong reputation, therefore we are looking for a motivated, dynamic and flexible Medical Writer to join our team.What is the job about?As a Medical Writer, you focus on...