Associate Director Regulatory Affairs Jobs in France

Job DescriptionAssociate Director Mechanical Engineering (Data Centres & Mission Critical)Location: Paris FrancePosition Type: PermanentSalary: Highly Competitive Executive Package BenefitsWork Arrangement: Flexible Working & Excellent Work-Life BalanceOur client is a leading international engineeri...

The Specialist Local RA & PV Network will act as Local Country Person Responsible for Pharmacovigilance and Regulatory Affairs (LCPPV/LCPRA) and serves as the primary local RA&PV representative to ensure compliance with national pharmacovigilance and regulatory requirements in Australia. This positi...

The Regional Medical Excellence Associate Director/Director will be dedicated to the Region Europe and main responsibilities are as follows:Contribute to the development of the Europe Region Medical strategies and tacticsProvide European Medical team with relevant insights medical practice understan...

Regulatory Affairs Intern(6 months - March 2027 - Lyon) We are looking for our new Regulatory Affairs Intern for a duration of 6 months based in Lyon.As a Regulatory Affairs Intern you will support the Regulatory Affairs team in ensuring regulatory compliance of medical devices and combination produ...

AbbVie HQ Europe is looking for an Associate Director International HTA Strategy Immunology. In this role you will shape evidence and value strategies that support access to AbbVies immunology medicines. You will connect HTA (Health Technology Assessment) insight asset strategy and cross-functional...

Revolution Medicines is a global commercial-state oncology company dedicated to discovering developing and delivering innovative medicines for patients with RAS-addicted cancers. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform the company is advancing a broad integrated portfoli...

About The Role The Regulatory Affairs Manager (REACH Expert) is a critical enabler of DKSHs Specialty Chemicals business across Europe ensuring regulatory compliance and strategic alignment with an evolving chemical regulatory landscape. This role combines REACH dossier management regulatory intelli...

About us - Unibail-Rodamco-Westfield (URW) is an owner developer and operator of sustainable high-quality real estate assets in the most dynamic cities in Europe and the United operate 65 shopping centres in 11 countries including 42 which carry the iconic Westfield brand. Our destinations attract o...

Job DescriptionKey ResponsibilitiesLead and develop the Regulatory Affairs team providing clear direction and people management.Develop and execute regulatory strategies to secure timely approvals and maintain optimal product positioning.Ensure timely submission approval and lifecycle management of...

IMPORTANT: after you apply please check your email. We send you a link to complete your application it is not considered until that last step is done. If you do not see it check your spam folder.This is a fully remote position open to candidates based in France.Pay: $50$80/hrRole Title: Regulatory A...

Résumé de la fonction :Participer à la définition de la stratégie et des lignes directrices de rédaction des dossiers CMC pharmaceutiques. Définir et réaliser les étapes de rédaction et de suivi des dossiers CMC règlementaire pharmaceutiques et des dossiers Qualité non-pharmaceutiques des nouveaux p...

We are looking for a hands-on and strategic Regulatory Affairs & Quality Assurance Specialist to help bring our technology from development to global commercialization. You will join our Compliance department (Quality Assurance Regulatory Affairs & Clinical Affairs) and report to the Head of Complia...

Résumé de la fonction :Participer à la définition de la stratégie et des lignes directrices de rédaction des dossiers CMC pharmaceutiques. Définir et réaliser les étapes de rédaction et de suivi des dossiers CMC règlementaire pharmaceutiques et des dossiers Qualité non-pharmaceutiques des nouveaux p...

If youre interested in this role please apply in English and include an English version of your Resume/CV.The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.M...

At Moodys we unite the brightest minds to turn todays risks into tomorrows opportunities. We do this by striving to create an inclusive environment where everyone feels welcome to be who they arewith the freedom to exchange ideas think innovatively and listen to each other and customers in meaningfu...

Au sein de notre département Affaires Réglementaires nous recherchons un(e) Regulatory Affairs Specialist pour un CDD de 6 mois dans le cadre dun remplacement de congé maternité. Vous jouerez un rôle clé dans le maintien de la conformité réglementaire de nos dispositifs médicaux et contribuerez acti...

Would you like to join an international team working to improve the future of healthcare Do you want to enhance the lives of millions of people Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in p...

Are you passionate about the pharmaceutical industry Would you like to contribute to a global program involving multiple sites around the world Would you like to be part of a fast-growing company If so you could be the person were looking for!A global leader in diabetology Novo Nordisk is an interna...