Regulatory Affairs Intern

Location: Meyrin, Geneva, CH- Division: - Division: Regulatory Affairs- Job Type: Permanent role We are recruiting a **Regulatory Affairs CMC Manager** at our headquarters and biotech production site in Geneva. Reporting to the Head of CMC, your mission is to provide expertise on regulatory CMC activities for initial registration in the context of...

An established industry player is seeking a Regulatory Affairs Specialist to enhance its portfolio across Europe. In this vital role, you will manage Regulatory Life Cycle activities, ensuring compliance and effective communication with local regulatory teams. You will also maintain Global Master Dossiers and contribute to regulatory policies, making a...

**Date**:9 oct. 2024 **Lieu**: Genève, Corporate, 1203 **Entreprise**:teoxanesa Teoxane Laboratories were established in Geneva, Switzerland, in 2003. They are specialized in the design and manufacturing of hyaluronic acid-based dermal fillers and dermocosmetics. Teoxane strength is to offer a global patient care. Using its products, practitioners are...

Description Our CompanyEFG International is a global private banking group, offering private banking and asset management services. We serve clients in over 40 locations worldwide. EFG International offers a stimulating and dynamic work environment and strives to be an employer of choice. EFG is committed to providing an equitable and inclusive working...

Our CompanyJOB DESCRIPTIONEFG International is a global private banking group, offering private banking and asset management services. We serve clients in over 40 locations worldwide. EFG International offers a stimulating and dynamic work environment and strives to be an employer of choice.EFG is committed to providing an equitable and inclusive working...

Medical Device - Regulatory Affairs Manager / Director - Pharma Responsibilities Establish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements. Training the team with EMEA / FDA requirements Qualifications Min 8 years in regulatory affairs in medical device Min 4 years as Regulatory Affairs...

Medical Device - Regulatory Affairs Manager / Director - Pharma Establish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements. Training the team with EMEA / FDA requirements Qualifications Min 8 years in regulatory affairs in medical device Min 4 years as Regulatory Affairs Manager Experience with...

As the Regulatory Affairs Specialist, you will play a critical role in enabling the PHC business for the relevant portfolio within and outside Europe. You will coordinate Regulatory Life Cycle Management activities across multiple countries, ensuring compliance with regulatory requirements and maintaining Global Master Dossiers. Additionally, you will...

Responsibilities - Play a key role in bringing innovative medical technologies to market - Collaborate with expert teams across product development and regulatory strategy - Contribute to the development and execution of product registration plans - Identify and compile documentation for regulatory submissions - Create submission dossiers and support...

Regulatory Affairs Specialist - Medical Devices - EUAnteris Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team.Our mission is to forge new frontiers in cardiac care by pioneering...