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il y a 1 jour
Brussels, Belgique MedTech Europe Temps pleinAbout This RoleWe are seeking an accomplished Director of Public Affairs to drive MedTech Europe's strategic engagement with European policy makers and other stakeholders. Reporting to the Director General for Corporate Affairs, this senior role offers the opportunity to shape policy positions, build influential partnerships, and position the medtech...
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Director of Public Affairs
il y a 1 jour
Brussels, Belgique MedTech Europe Temps pleinAbout This RoleWe are seeking an accomplished Director of Public Affairs to drive MedTech Europe's strategic engagement with European policy makers and other stakeholders. Reporting to the Director General for Corporate Affairs, this senior role offers the opportunity to shape policy positions, build influential partnerships, and position the medtech...
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Director of Public Affairs
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Brussels, Belgique MedTech Europe Temps pleinAbout This RoleWe are seeking an accomplished Director of Public Affairs to drive MedTech Europe's strategic engagement with European policy makers and other stakeholders. Reporting to the Director General for Corporate Affairs, this senior role offers the opportunity to shape policy positions, build influential partnerships, and position the medtech...
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Brussels, Belgique WhatJobs Temps pleinDirector / Senior Manager Regulatory Affairs – CropLife Europe Location: Brussels, Belgium Company Overview: CropLife Europe (CLE) is the voice of the crop protection sector in Europe. We represent 26 market‑leading companies and National Associations in 32 countries. Members include global companies, SMEs, and national associations in conventional...
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Public Affairs Director
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Brussels, Belgique WhatJobs Temps plein1 day ago Be among the first 25 applicants Forward Global is an international risk and reputation management advisory firm delivering custom solutions for clients worldwide. Our clients include global corporations, trade associations, law firms, private equity and venture capital firms, foreign governments and sovereign wealth funds, international...
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Regulatory Affairs Manager
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Brussels, Belgique CareForce One Temps pleinGreat opportunity for a Regulatory Affairs Manager to join the Belgian affiliate of a mid-size pharmaceutical company that recently acquired new molecules, mainly Orphan Drugs / Oncology.JOB SCOPE:You will be the key partner to the local organization for all Regulatory (RA) and some Pharmacovigilance (PV) / Patient Safety matters. This is a great opportunity...
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Public Affairs Director
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Public Affairs Director
il y a 3 semaines
Brussels, Belgique European Plastics Converters | EuPC Temps pleinAbout EuPCEuropean Plastics Converters (EuPC) is the EU-level trade association representing theinterests of plastics converting companies in Europe. Based in Brussels, EuPC bringstogether national plastics associations and European sectoral organisations, representingmore than fifty thousands converting companies that supply plastic products into key...
Director of Regulatory Affairs
il y a 3 semaines
Director Regulatory Affairs, EuropeRare Disease BiologicsEMA Filings Experience RequiredRemote position- time in HQ in Europe will be required for business critical requirements.** Please note candidates must live in Belgium to be considered **About the CompanyWe are working with a European biotech organisation, who are developing novel therapeutics for a range of rare diseases. They have achieved FDA success with a few of their programs, which are now launching into further markets around the world. The portfolio ranges from preclinical to approved products, with multiple new indications currently being explored. We are looking for a Director EU Regulatory Affairs to support on a number of new indications, from early to late phase development & lifecycle management. You will report into the Head of Regulatory Affairs, Europe & International Markets.About the RoleThis role is an exciting opportunity to join as a key member of the EU & International regulatory team and will be working on a number of indications spanning early & late phase development, and lifecycle management. This will include providing hands-on contributions to MAAs across Europe, including EMA, MHRA and Swiss Medic. The role provides a critical contribution to the development of product regulatory strategies for different indications and will be a key advisor and enabler of successful product launches and commercialization activities.We are looking for candidates who have the below experience:Experience of working on regulatory strategy for late phase compounds- this must include MAA filings to the EMA.EMA experience is required, additional experience with MHRA or Swiss Medic would be beneficial.Experience in orphan drugs or novel first-in-class/ best-in-class indications would be highly beneficialPharma or biotech experience is required, any experience in rare disease & unmet medical need would be advantageousStrong knowledge in overall drug development & the biopharma regulatory landscapeA willingness to work operationally and "hands-on" when required to get tasks completedA desire to work in a biotech environment which can be fast-paced & demanding, whilst also being able to adapt to any strategic changes in pipeline direction.Please apply with an up to date CV for consideration.
