Regulatory Affairs CMC Consultant

OverviewRegulatory Affairs CMC Officer – Paris, France (F/M) role at Alsinova, the CRO subsidiary of the Astek Group. Alsinova is currently recruiting a Regulatory Affairs CMC Officer to strengthen its regulatory affairs team and support strategic projects in the pharmaceutical industry.Your MissionWorking closely with our clients in the Life Sciences...

Cookie Notice**Title:**Senior Manager CMC Regulatory**Company:**Ipsen Innovation (SAS)**About Ipsen:**Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France...

Title: Senior Manager CMC Regulatory Company: Ipsen Innovation (SAS) About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.S., France and the U.K, we...

Job TitleSenior Manager, CMC Regulatory Strategy BiologicsDivision / FunctionGlobal Regulatory Affairs (GRA)Manager’s Job TitleDirector/Sr Director CMC Regulatory Strategy BiologicsLocationParis, FR & Paddington, UKJob SummaryResponsible for developing and executing CMC regulatory strategy across product lifecycle—from early clinical trials to marketing...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...

Vos missions Vous interviendrez au sein d’un département Réglementaire CMC afin d’apporter une expertise de haut niveau sur les aspects réglementaires CMC liés aux dispositifs médicaux et produits combinés, dans un contexte de développement international. Fournir un avis d’expert sur les aspects réglementaires CMC applicables aux dispositifs...

A leading MedTech recruitment firm is seeking a Senior Regulatory Affairs Consultant to develop and execute regulatory strategies that align with global requirements. The role requires 5-7 years of regulatory experience within medical devices, expertise in leading FDA submissions, and a solid grasp of project management. This position offers the opportunity...

🔎 Title: Senior Regulatory Affairs Consultant🔸 The CompanyIf you are a QA/RA professional with an interest in innovation and groundbreaking development, we have an incredible role for you. This is a chance to join an established midsize Software as a Medical Device company.🔹 As a Regulatory Affairs Consultant your mission is to:Develop and execute...

OverviewVous avez un profil solide en Affaires Réglementaires, une expertise confirmée en CMC, et souhaitez intégrer une structure dynamique au cœur de l'innovation en Life Sciences ?Rejoignez-nous !Rattaché·e au département Affaires Réglementaires, vous jouerez un rôle clé dans la mise en place et la coordination de la stratégie réglementaire...

A leading pharmaceutical company is seeking a Senior Manager for CMC Regulatory Strategy Biologics. This role involves developing and executing CMC regulatory strategies for product lifecycle management. Responsibilities include leading dossier preparation, engaging with regulatory authorities, and coaching junior staff. Candidates should have 8-10 years of...