IVDR Regulatory Affairs Specialist

Regulatory Affairs Officer – IVDR ComplianceAlsinova, a subsidiary of the Astek Group, is a consulting firm specialized in Life Sciences. We support pharmaceutical, biotech, and medtech companies by providing high-level expertise in regulatory affairs, clinical development, data, quality, and pharmacovigilance. To support one of our major partners in the...

A consulting firm is seeking a Regulatory Affairs / Clinical Affairs Specialist in Lyon to manage regulatory projects in pharmaceuticals and medical devices. The role involves advising clients on compliance, preparing regulatory submissions, and monitoring changes in regulations. Candidates should have 5-15 years of experience in regulatory affairs, strong...

We are looking for a Regulatory Affairs / Clinical Affairs Specialist with strong experience in pharmaceuticals and medical devices. Manage regulatory projects in pharmaceuticals and medical devices Advise clients on regulatory compliance, product registration, and market access Prepare and submit regulatory dossiers to competent authorities Monitor...

Select how often (in days) to receive an alert: Title: Specialist, Safety Data Sheet Europe Location: Lyon, FR, FR Global Business Unit: PM Job Function: Regulatory Services Requisition Number: 239625 Description: About The Role The Specialist, Chemical Product Safety Europe is responsible for ensuring the compliance, classification, labelling and safety...

Manager Affaires Réglementaires & Distribution Export Spécialiste de l'industrie Pharmaceutique et des Dispositifs Médicaux, VIQI rassemble des passionnés ne souhaitant évoluer qu’auprès des industriels œuvrant pour la santé des patients. Pour l'un de nos clients leader dans l'industrie des Dispositifs Médicaux, nous recherchons un(e) Manager...

RejoignezExcelya, où l'audace, l'attention portée aux autres et l'énergie définissent notre identité et notre manière de travailler. Nous croyons en la création de solutions ambitieuses et en un environnement inclusif, où la collaboration et le développement individuel vont de pair. Dans le cadre d'une nouvelle prestation, nous...

Work Flexibility: Hybrid or OnsitePourquoi rejoindre Stryker?Vous cherchez un endroit qui valorise vos talents uniques ? Découvrez la culture primée de Stryker.Nous sommes ravis de vous présenter une nouvelle opportunité de rejoindre Stryker en tant que Staff Specialist, Regulatory Affairs, basé(e) à Décines-Charpieu !Le/La Staff Specialist,...

About The Role The Specialist, Chemical Product Safety Europe is responsible for ensuring the compliance, classification, labelling and safety documentation of chemical products distributed by DKSH across the European Union, the United Kingdom, and Switzerland. Embedded within a 12-person regulatory team, this position plays a critical role in protecting...

**About The Role** The **Specialist, Chemical Product Safety Europe** is responsible for ensuring the compliance, classification, labelling and safety documentation of chemical products distributed by DKSH across the European Union, the United Kingdom, and Switzerland. Embedded within a 12-person regulatory team, this position plays a critical role in...

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

Regulatory Affairs Specialist (Freelance) Location: Lyon, France (hybrid) Length: 12 months (possibility of extension) Hours: Full-time (40 hours per week) Start Date: Mid-August - September 2026 Engagement: Freelance Key Responsibilities Contribute to the development and maintenance of regulatory strategies for both existing...