Responsable Affaires Réglementaires - spécialiste produits combinés

As an RA (Senior) Consultant , you will play a pivotal role in supporting pharmaceutical and medical device clients in the development, submission, and lifecycle management of drug-delivery devices and combination products. You will lead and guide a variety of regulatory projects, providing expert advice on regulatory strategies, classifications, and pathways, while collaborating closely with R&D teams to develop new products or manage the lifecycle of authorized ones.

You will be responsible for the end-to-end regulatory support and will contribute significantly to the successful market entry and maintenance of combination products in key regulatory regions, including the EU and US.

Key responsibilities include :

• Leading and implementing the regulatory strategy development for drug-delivery devices and combination products.
• Providing guidance on regulatory classification and submission pathways for the EU (MDR, CE Marking) and the US (FDA, 510(k), PMA, NDA, BLA, ANDA).
• Supporting R&D teams in the development phase, from design control to quality management, ensuring compliance with applicable technical standards and regulatory frameworks.
• Liaising with key internal stakeholders, including RA CMC, Manufacturing, Clinical Development, and Marketing, to compile dossiers and technical documentation for regulatory submissions.
• Drafting / reviewing relevant device sections of eCTD modules (e.g. 3.2.R, 3.2.P.2) for combination products applications
• Managing communications with notified bodies and health authorities, including participation in audits and inspections.
• Mentoring other consultants and sharing knowledge within the team, contributing to internal training and development

Your Profile :

You are an independent and proactive professional with a passion for contributing to cutting-edge regulatory projects. You thrive in dynamic environments and are adept at adjusting to clients' needs while ensuring high-quality regulatory outcomes. You are eager to continually learn and share knowledge with both clients and internal teams, demonstrating a strong commitment to your professional development.

You possess :

• Min 8–12 years of relevant experience in Regulatory Affairs and / or R&D related to :
• Drug-delivery devices (e.g., pre-filled syringes, autoinjectors, dry powder / metered dose inhalers, oral / nasal vaccines, blow-fill seals).
• Combination products under EU (MDR, CE Marking, Notified Body Opinion) and / or US (FDA, 510(k), PMA, NDA, BLA, ANDA) regulatory frameworks.
• Quality Management Systems for medical devices and combination products (ISO 13485, MDR, 21 CFR 820 / QSR / QMSR, ISO 14971 ).
• Solid expertise in the development of devices under design controls and familiarity with technical standards applicable to drug-delivery devices.
• Experience in supporting R&D teams through the development phases of combination products.
• Ability to independently manage projects and stakeholder relationships, leading regulatory strategies for multiple clients in parallel.
• Experience working cross-functionally with RA CMC, Manufacturing, Clinical, and Commercial teams to compile technical documentation and regulatory submissions.
• Proven experience in handling NB / FDA / NCA audits and inspections.
• University degree in Biomedical Engineering, Pharmacy, Health Technology, Medical Science, or another relevant field.
• Fluency in English (required) and French (desired).