Regulatory Writer
il y a 5 jours
Project OverviewProject Type: Regulatory Writing (Submissions)Location: Europe, Fully Remote - UK PreferredContract Type: Permanent, Full-TimeIdeal Start Date: ImmediatelyKey ResponsibilitiesLead, mentor, and develop regulatory writers, providing guidance on client issues and supporting knowledge sharing across the team.Serve as primary contact for designated projects, overseeing scientific and technical quality and ensuring alignment with client expectations.Manage delivery of multiple projects, meeting quality standards, timelines, and budgets while tracking scope in partnership with Project Management.Contribute to regulatory writing training and support line management responsibilities as needed.Provide strategic input on complex programs (e.g., submissions), advising on regulatory writing processes, best practices, and client procedures.RequirementsStrong technical and scientific capabilities with a proven track record in delivering high‐quality regulatory documents.Excellent communicator with the ability to coach and mentor junior team members on client and project‐related challenges.Skilled at managing multiple projects and consistently producing clear, accurate, and well‐written deliverables within deadlines.Proactive in sharing knowledge and supporting team development to strengthen overall capability and collaboration.If this role is of interest to you, please apply directly to learn more. If not, feel free to share with your network.#J-18808-Ljbffr
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Senior Regulatory Writer | Remote Europe
il y a 5 jours
Brussels, Belgique EPM Scientific Temps pleinA leading scientific consultancy is seeking a Regulatory Writing Lead to oversee a team of writers and ensure high-quality submissions. This position is fully remote, ideally for candidates based in Europe. The candidate should have a strong background in regulatory writing, excellent communication skills, and the ability to mentor junior team members....
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Senior Principal Medical Writer – Oncology Regulatory Lead
il y a 6 jours
Brussels, Belgique Syneos Health, Inc. Temps pleinA leading biopharmaceutical solutions organization in Belgium is seeking a Senior Principal Medical Writer to develop regulatory documents for submissions globally. The candidate will manage projects and mentor junior staff, ensuring compliance with regulatory guidelines. This role requires strong communication and project management skills, with a focus on...
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Senior Principal Medical Writer
il y a 6 jours
Brussels, Belgique Syneos Health, Inc. Temps pleinSenior Principal Medical Writer - Regulatory - Oncology - Single SponsorUpdated: October 2, 2025Location: Brussels, VAN, BelgiumJob ID: 25101798-OTHLOC-3532-2DRDescriptionSenior Principal Medical Writer - Regulatory - Oncology - Single SponsorSyneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer...
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Regulatory Affairs Manager
il y a 2 semaines
Brussels, Belgique MSD Temps pleinThe Senior Regulatory Affairs Manager (RAM) has as primary task to take care of the several Regulatory Affairs (RA) activities of the RA-QA-PV Unit. For the Reg Affairs Manager this means the life cycle management of a group of product registrations of MSD AH Benelux. This life cycle management involves translation of product information texts and taking...
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(Senior) Specialist, Regulatory Affairs
il y a 6 jours
Brussels, Belgique MSD Temps plein**R321324 (Senior) Specialist, Regulatory Affairs** **Function description** The (Senior) Regulatory Affairs Manager (RAM) has as primary task to take care of the several Regulatory Affairs (RA) activities of the registered veterinary medicinal products for The Netherlands, Belgium and Luxembourg. For the RAM this means the life cycle management of a group...
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Quality Assurance Specialist
il y a 2 semaines
Brussels, Belgique Vivid Resourcing Temps pleinJob Title: Quality EngineerLocation: BrusselsRole Type: Onsite/HybridSalary: Up To €70,000Overview:The Quality Engineer ensures the qualification and maintenance of manufacturing equipment, utilities, facilities, and automated systems, guaranteeing compliance with regulatory standards and maintaining a state of validated operations.Key...
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Quality Assurance Specialist
il y a 4 semaines
Brussels, Belgique Vivid Resourcing Temps pleinJob Title: Quality EngineerLocation: BrusselsRole Type: Onsite/HybridSalary: Up To €70,000Overview:The Quality Engineer ensures the qualification and maintenance of manufacturing equipment, utilities, facilities, and automated systems, guaranteeing compliance with regulatory standards and maintaining a state of validated operations.Key...
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Analyste Fonctionnel Senior
il y a 2 semaines
Brussels Metropolitan Area, BRU, Belgique BK CONSULTING BeNeLux Travail à distance Temps pleinBased on solutions designed by the Lead Analyst, you translate functional and non-functional requirements into detailed analysis for small to medium-sized features related to processes and systems within your domain. You contribute to solution quality, system stability, regulatory compliance, and continuous improvement with a strong client-centric...
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Business Functional Analyst – Banking
il y a 2 semaines
Brussels Avenue Marnix 13-15, Belgique Deutsche Bank Temps pleinJob Description:For over 150 years, our dedication to being the Global Hausbank for our clients has been driven by our people – in around 60 countries and across more than 150 nationalities. Their deep understanding, insights, expertise and passion help our clients navigate an increasingly complex world – be it in our Corporate Bank, our Private Bank,...
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Business Functional Analyst – Banking
il y a 2 semaines
Brussels Avenue Marnix 13-15, Belgique Deutsche Bank Temps pleinJob Description:For over 150 years, our dedication to being the Global Hausbank for our clients has been driven by our people – in around 60 countries and across more than 150 nationalities. Their deep understanding, insights, expertise and passion help our clients navigate an increasingly complex world – be it in our Corporate Bank, our Private Bank,...
