Regulatory Affairs Specialist

Leader européen dans le domaine des lubrifiants pour l’aéronautique et expert dans le développement et la fabrication d’esters synthétiques de hautes performances, nous recherchons **un/une Regulatory Affairs Specialist**, qui travaillera sous la responsabilité du Directeur du service. Le/la Regulatory Affairs Specialist devra assurer les missions...

**We are Growing**! Let us support your career journey the Biorasi way. Innovative, Collaborative, Dynamic and Evolving. Capitalizing on your strengths while encouraging work-life balance. Biorasi is an award-winning, customer-focused, full-service clinical research organization, and we are unlike any CRO you’ve ever heard of. Biorasi is looking for top...

IFF applies expert science to advance market-driven, healthy and sustainable solutions for the food, beverage, dietary supplements, and many other industries. IFF is growing and we are looking for a dedicated and passionate individual to join our Regulatory Affairs team in EMEA! In the Regional Regulatory Affairs Team in EMEA we have an opening for a...

Nanobiotix is happy to welcome a CMC manager, regulatory affairs to provide valuable support to our mission to advance groundbreaking nanomedicine solutions. At the forefront of pioneering nanomedicine approaches that could redefine cancer treatment, our team at Nanobiotix is dedicated to creating innovative solutions to impact countless lives across the...

**Job title**:Specialist Regulatory Affairs (12 months) **City, country**:Neuilly sur Seine, France **Work mode**:Onsite At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work to not only benefit our People, Customers & Communities but also drive value. Equal access to...

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...

**Your responsibilities** - Maintaining the Technical Documentation for Medical Devices with support of other functions - Becoming familiar with regulations and standards applicable to specific areas of responsibility, which may include notified body exposure - Support product registrations including document management - Support the Medical Device team in...

In the context of a new project, we are looking for a Regulatory Affairs Officer in medical devises to join our teams in Paris. **Responsibilities**: Write the dossiers and coordinate with the different contributors (R&D, Production, QA, Clinical,..) Ensure that the constitution of the registration dossiers is in accordance with the new European regulation...

DescriptionAbout your roleWe are looking for a motivated and detail-oriented Regulatory Affairs Officer - Veterinary Medicines to join our team for an 18-month temporary position. In this role you will be responsible for supporting the maintenance of marketing authorizations (MA) in various regions. Your focus will initially be on the EU region, with...

**Summary**: **Key Responsibilities**: - Develop, implement, and manage regulatory strategies to ensure compliance with applicable regulations and standards. - Monitor changes in relevant regulatory environments, interpret new and existing regulations, and communicate potential impacts to key stakeholders. - Provide expert guidance on regulatory matters...