Senior European Regulatory Affairs Specialist

The Position Coordinating and supporting all regulatory activities to maintain registrations and to obtain new marketing authorisations for the company portfolio / pipeline subject to EU procedures across therapeutic areas. The position also requires strong project management skills to oversee regulatory initiatives, manage timelines effectively, and...

We are recruiting a Regulatory Affairs Specialistfor a global not-for-profit organization in Paris. Your tasks: - Coordinate with the team to plan, organize and submit regulatory submissions to national Health Authorities - Address regulatory queries from notifying bodies, Health Authorities and distributors and maintain regulatory approvals - Ensure that...

Excellent knowledge of EU regulatory medical device guidelines - Previous global experience within the pharmaceutical/medical device industry within Regulatory Affairs - Excellent written and verbal communication skills in English To strengthen our RA team based in Paris, we are seeking a Global Regulatory Affairs Specialist. This role is full time,...

Ecolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a **Senior **Regulatory Affairs Specialist**.** We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products....

Our client is a pioneering MedTech company based in Paris, developing Class III active implantable devices. With strong clinical adoption, regulatory approvals underway in Europe and the US, and plans for rapid growth, they are entering a new phase of expansion and are looking to hire a Senior Manager of Quality & Regulatory Affairs.The roleAs Senior Manager...

**Description générale**: **_ HRA Pharma Rare Diseases_** is dedicated to bringing the best care and services to people living with rare diseases and is committed to supporting healthcare professionals all over the world. We have over 15 years’ experience in rare and ultra-rare diseases with a portfolio of medicines that address Cushing’s syndrome and...

We are partnered with a Global Consumer Health Business, looking for a Regulatory Affairs Assistant for their International Regulatory Affairs Team.ResponsibilitiesPrepare and compile documentation for product registrations, renewals, and variations.Coordinate submissions with local authorities and track progress.Manage administrative tasks such as...

Senior Manager, Global Regulatory AffairsJoin to apply for the Senior Manager, Global Regulatory Affairs role at IpsenSenior Manager, Global Regulatory AffairsJoin to apply for the Senior Manager, Global Regulatory Affairs role at IpsenSummary Of The RoleTo be accountable for the strategy, tactics and implementation of all regulatory aspects of the assigned...

Regulatory RIMS Specialist - Life Science - 6-Month Contract - France/UK  This is a unique opportunity for a Regulatory RIMS Specialist to join our client – an esteemed partner for regulatory and compliance in healthcare. This is a contract opportunity of at least 6 months within the stunning city of Paris/London. With a globally established presence...

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...