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📑 Regulatory Affairs Officer Global Registrations Animal Health Human Health Contract Manufacturing Belgium Over KELA KELA, opgericht in , is een Belgische farmaceutische bedrijvengroep. KELA is een betrouwbare ontwikkelaar, producent en verdeler van veterinaire ...

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📑 Regulatory Affairs Manager M/F ...

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📑 Head of Regulatory Affairs Benelux Aspen Pharma Group 2023-07-07 Belgium Job Ref #: AP-4195 Industry: Pharmaceutical And Medical/Healthcare Job Type: Permanent Positions Available: 1 Applications are invited for the above indicated vacancy t ...

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📑 About the job We are seeking for a Regulatory Affairs Officer/Specialist responsible for ensuring the delivery of regulatory activities performed on the Benelux market. About us Group 10 Responsibilities Ensure that the regulatory tasks and functions within the Regulato ...

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📑 Regulatory Affairs Specialist M/F <sp ...

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📑 **The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.** **• Prov ...

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📑 Regulatory Affairs Expert in Animal Health – Pharmaceuticals – Brussels – 12 Months Do you want to be involved with exciting Pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of E ...

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📑 You manage the regulatory activities for a diverse range of products, including but not limited to: prepare, submit and follow-up regulatory submissions (BLA, CTD, NDA,…), assess post-approval changes, manage responses to the Board of Health, review of packaging/inserts… You collaborate closely with the Regulatory Affairs team and o ...

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📑 Insulet started in 2000 with an idea and a mission to enable our customers to enjoy simplicity, freedom and healthier lives through the use of our Omnipod® product platform. In the last two decades we have improved the lives of hundreds of thousands of patients by using innovative technology that is wearable, waterproof, and lifestyle accommodat ...

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📑 Job Description: Responsibilities: Regulatory intelligence: Keep track of and evaluate regulatory updates, legislative changes, and industry-specific guidelines related to chemicals.Risk Assessment: Determine the impact of regulatory changes on the organization's operations, products, and se ...

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📑 Who We Are It takes a village, and at BioMarin our corporate groups are the people behind our success. Groups such as IT, Finance, Legal, Global Compliance & Ethics, and our People Team provide foundational support of all areas of operation at BioMarin. Manager, Government Affairs EUCAN Summary The Manager, Governm ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Medical Affairs Consultants to join our consulting team for clients' projects (from big pharma to small biotech) based in Belgium. This job description is an example on how your job could look like . Once we have a ...

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📑 Client Description: Vast Contract Regio Evergem #regulatory #affairs #coordinator #chemistry Beschik je over een masterdiploma in een wetenschappelijke richting (voorkeur chemie)? Heb je enkele jaren werkervaring binnen Regulatory Affairs? Ben je leergierig, zelfstandig en beschik je over een sterk analytisch ...

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📑 Be a part of a revolutionary change. At Philip Morris International, we’ve chosen to do something incredible. We’re transforming our business and building our future on smoke-free products with the power to deliver a smoke-free future. With huge change, comes huge opportunity. So, wherever you join us, you’ll enjoy the freedom to dream up and deliv ...

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📑 When our values align, there's no limit to what we can achieve. We are seeking an experienced Regulatory Affairs Consultant to join our team. As a Regulatory Affairs Consultant, you will be responsible for providing expertise in registration Regulatory Affairs, with a focus on Global Regulatory (Clinical/Safety) an ...

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📑 When our values align, there's no limit to what we can achieve. We are seeking an experienced Regulatory Affairs Consultant to join our team. As a Regulatory Affairs Consultant, you will be responsible for providing expertise in registration Regulatory Affairs, with a focus on Global Regulatory (Clinical/Safety) an ...

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📑 Description Kenvue is currently recruiting for: Regulatory Affairs Associate This position reports to the Head Of Regulatory Affairs Benelux and is based in Antwerp (Belgium). Who we are At Kenvue , we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we're the ...

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📑 As the successful Regulatory Affairs Specialist, you will have the following responsibilities:Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on EuropeCollect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, an ...

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📑 As a successful Regulatory Affairs Specialist - Pharma - BeNeLux you will have the following responsibilities:Prepare, submit, maintain and record technical and regulatory documentationEnsure up to date EMEA document management systemCollect information on products to create and update the product regulatory informa ...

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📑 Senior Legal Counsel - Regulatory Law EMEA - 2406180718W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Thr ...

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📑 Senior Legal Counsel - Regulatory Law EMEA - 2406180718W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Thr ...

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📑 About the Role What you'll doLead the implementation of ISO 14001 (Environmental Management System standard) in with the support of colleagues from the Quality TeamMaintain a thorough understanding of new and existing European environmental and chemicals regulations (hazardous substan ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Technical Regulatory CMC Writers to join our consulting team for clients (from big pharma to small biotech) based in Belgium . This job description is an example on how your job could look like. Once we have a spec ...

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📑 For the expansion of our regulatory team, argenx is looking for an Associate Director/Director Regulatory Affairs, argenx, based in Europe, to support the rapid growth needed for successful commercialization.Key Accountabilities and Responsibilities:The Associate Director/Director Regulatory Affairs is a key member of the gl ...

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📑 Job Description Keyrus Life Science is looking on a regular basis for Regulatory Affairs Consultants to join our consulting team for clients (from big pharma to small biotech) projects based in Belgium. This job description is an example on how your job could look like. Once we have a specifi ...

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📑 For our Diabetes Care division, we are recruiting a Senior Regulatory Specialist for Benelux. The Senior Regulatory Specialist is responsible for managing an efficient program to ensure that all regulatory activities for Abbott Diabetes Care products are achieved to an agreed schedule. Role and Responsibilities ...

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📑 SANOFI CHC PURPOSE AND ASPIRATION JOB PURPOSE The Regulatory Science, Policy and Intelligence Lead directly lead and manage the CHC Global Regulatory Affairs, Policy, and Intelligence related activities. The head will provide thought leadership to bring Scientific Affairs to the forefront of building gl ...

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📑 Join Our Team as a Senior Regulatory & Public Affairs Manager (M/F/X) Are you passionate about shaping the future of energy transition? Do you thrive in a dynamic environment where your expertise can drive positive change? Look no further! ENGIE Belgium is actively seeking a Senior Regulatory & Public Affairs Manag ...

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📑 Goodyear. More Driven. The opportunity The Head of Public Affairs EMEA is responsible for supporting the EU-wide implementation of the EMEA Public Affairs strategy, with a specific focus on France and Luxembourg, to advance and protect Goodyear's business objectives. The Head of Public Affairs EMEA will ...

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📑 About the Role Become part of the Legal & Compliance team The Legal & Compliance team is looking for a Regulatory Affairs Specialist with a strong background in payments, securities, and technology policy. As part of the Regulatory Affairs team, you will take responsibility for financial and technology policy ...

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📑 For the expansion of our EMEA team, argenx is looking for a Head of Regulatory Affairs, EMEA.argenxargenx is a fast-growing global immunology company committed to improving the lives of people suffering from severe autoimmune diseases. Thanks to colleagues based in Europe, the United States and Japan, we translate immunology b ...

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📑 Make your mark for patients We are looking for a Regulatory CMC Scientist – Small Molecules to join us in our Regulatory Affairs team, based in any of the following locations: Brussels (Belgium) or Slough (UK) About the role Define the strategy, planning and preparation (writing ...

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📑 Our client, a pharmaceutical company based in Belgium is looking for a (Junior) Regulatory Affairs Specialist a to come on board and join their team. T ...

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📑 Key Accountabilities and Responsibilities:Leads the CMC Regulatory Affairs function within post-marketing CMC. Provides strategic leadership to support argenx’ portfolio marketed products for local and global filings. The candidate will be responsible for assuring development and execution of regulatory strategi ...

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📑 BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: ...

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📑 Make your mark for patients We are looking for a Head of Global Labelling, Promotion & Advertisement to join us in our Global Regulatory Affairs team, based in either our Brussels, Belgium or Atlanta, Georgia (U.S.) offices. About the role The Head of Global Labelling & Promotion ...

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📑 Unveil Your Expertise as an Ecotoxicologist – Join a Leading Force in Scientific Innovation (Brussels Area) Do you possess a relentless passion for environmental safety and a keen eye for regulatory compliance? Are you a collaborative team player who thrives in a culture that fosters creativity and scienti ...

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📑 Introduction For our client in Zaventem we are looking for a SR. Associate Regulatory Affairs s who will provide regulatory guidance and support for regional and global veterinary biological maintenance teams and development project teams. Job description The Sr Asso ...

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📑 Qarad Belgium, The Netherlands Regulatory affairs Table of Contents Qarad, part of the QbD group, is a fast-growing consultancy company assisting manufacturers of In Vitro Diagnostics (IVD) and Medical Devices (MD) in coping with European and other regulations. Our object ...

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📑 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 ...

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📑 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 ...

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📑 **Position Summary** As a Medical Affairs Advisor, your main responsibility will be to lead the development and implementation of the medical strategy to support our business portfolio and establish Nestlé Health Science as a leader in scientific knowledge and credibility among healthcare professionals (HCPs). ...

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📑 The Manager, Regulatory Affairs International supports ambitious geographical expansion plans. The position will support registration of existing portfolio products into new territories and to register several of development projects into the international region. This role is key to driving both the Regulatory strategy and execution.• ...

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📑 GOVERNMENT AFFAIRS MANAGER **At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.** **Job Overview** **This Role is a remote position in Belgium, the Netherlands or Germany.** ...

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📑 Scientific and Regulatory Affairs Specialist Corporate division Location: Brussels or Hoofddorp About L’Oréal L'Oréal has been a world leader in the cosmetics business for more than years and has grown into one of the largest FMCG companies in the world. With international bran ...

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📑 Job Description Our client is a global medical device company, a pioneer of the MR-guided focused ultrasound technology which is a game-changing innovation. They are looking for a Clinical Affairs Program Manager Europe. The role is % remote with up to 40% travel and based in Europe. As part of the global cl ...

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📑 **Overview:** We are seeking an experienced and dedicated Medical Advisor to join our team. In this role, you will be at the forefront of providing expert medical guidance. Your expertise will contribute significantly to the development, promotion, and compliance of medical products and practices. **Responsibilities:** ...

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📑 FunctieomschrijvingAls Regulatory Affairs Expert zal je verantwoordelijk zijn voor : het beheren van regelgevingskwesties het waarborgen van naleving van wet- en regelgeving met betrekking tot de producten en activiteiten samenwerking met interne teams en externe belanghebbenden o ...

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📑 POSITION SUMMARY: Reporting to the VP Global QA, the Director of Quality Assurance and Regulatory Affairs – EMEAA, provides technical, compliance, and regulatory guidance to processing facilities within Europe and Asia and has responsibility for the quality oversight of Sterigenics’ quality system implementation and execution.< ...

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📑 **Senior Director, Public Policy** at GitLab Remote The GitLab DevSecOps platform ( empowers 100,000+ organizations to deliver software faster and more efficiently. We are one of the world’s largest all-remote companies ( ...

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