Director, Regulatory Affairs

THE COMPANY Join a "Made in France" company and become a specialist in in vitro diagnostics. A human-sized company with a global reach, present in more than 120 countries worldwide. Dynamic with a large number of rapidly expanding projects, resulting in the opening of new subsidiaries every year! Their mission is to provide powerful tools that translate what...

**Position**: The Company Moët Hennessy is the Wines and Spirits division of LVMH. The world leader in luxury wines and spirits, Moët Hennessy is internationally renowned for its exceptional and exclusive brands. These include Dom Pérignon, Moët & Chandon, Veuve Clicquot, Krug and Ruinart for champagne; Hennessy, Belvedere, Glenmorangie, Ardbeg and...

Quelles sont les missions ?Act as the Primary PRRC for Regulatory for the EMEA and LATAM regions: - Lead the Regulatory Affairs Registrations team for approvals and product registrations of all medical devices;- Planning and executing all aspects of Regulatory Affairs and acts as the company's regulatory representative;- Develops, approves, and implements...

Quelles sont les missions ?Act as the Primary PRRC for Regulatory for the EMEA and LATAM regions: - Lead the Regulatory Affairs Registrations team for approvals and product registrations of all medical devices;- Planning and executing all aspects of Regulatory Affairs and acts as the company's regulatory representative;- Develops, approves, and implements...

Poste : Act as the Primary PRRC for Regulatory for the EMEA and LATAM regions: - Lead the Regulatory Affairs Registrations team for approvals and product registrations of all medical devices;- Planning and executing all aspects of Regulatory Affairs and acts as the company's regulatory representative;- Develops, approves, and...

**Associate Manager Regulatory Affairs** Kendo Brands, the Beauty and Skincare brand incubator of the LVMH Group, has now become a reference in terms of creativity and innovation. Through their business expertise, their sharp knowledge of the market and their ability to always renew themselves in an extremely dynamic universe, Kendo teams are disrupting the...

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...

On-site presence in the South of France once per month for 2-3 days. Stirling Q&R, a leading recruitment company, is currently assisting our esteemed client in the search for a highly experienced Senior Manager/Associate Director, Regulatory Affairs. Our client, a renowned global biotech company specializing in oncology, is dedicated to improving treatment...

Nanobiotix is excited to announce an opening for a CMC Manager, Regulatory Affairs to join their team. In this role, you will play a crucial part in supporting Nanobiotix's mission to advance innovative nanomedicine solutions that have the potential to redefine cancer treatment.Specializing in the development and production of nanoparticles that enhance the...

Regulatory Affairs Officer / Linguistic Review Coordinator M/F - 025 EuropeRegulatory AffairsPermanent contractRegulatory Affairs Officer / Linguistic Review Coordinator M/F - 025 To ensure and coordinate the Linguistic Review (LR) for the Centralized products of one of our key clients, we are urgently looking for a Regulatory Affairs Officer / Linguistic...

**ROLE CONTEXT** Our Strategic Communications division in Paris is currently seeking a Director in France in the Public and Government Affairs (PGA) Practice, possibly with a strong focus on one of our key sectors: Healthcare & Life Sciences, Energy, Technologies, or Financial Services. We help our clients create sustainable relationships with policy...

Regulatory Affairs Specialist 362 In the frame of a project for one of our Top Clients, we are seeking for a Regulatory Affairs Specialist ( pharmacist ) responsible for ensuring the delivery of regulatory activities performed onsite in Paris region. About us Group 10 Responsibilities Under the responsibility of the regulatory coordinator of this...

I am partnered with a rapidly growing small medical device company who are looking for their first Director of Clinical Affairs. As the key leader in our clinical affairs group, you will play a crucial role in the development, execution, and success of a ground-breaking implantable device. This is a home-based position which will initially be a contract...

We are thrilled to be one of Deloitte's 500 fastest growing technology companies in the US - and now, we are ready to take our success to the next level by going public! This is an incredible opportunity to join our team as a Quality Assurance/ Regulatory Affairs AssociateSpecialist and help us reach new heights. At Allurion, our core values of Audacity,...

We are thrilled to be one of Deloitte's 500 fastest growing technology companies in the US - and now, we are ready to take our success to the next level by going public! This is an incredible opportunity to join our team as a Quality Assurance/ Regulatory Affairs AssociateSpecialist and help us reach new heights. At Allurion, our core values of Audacity,...

Regulatory Affairs Specialist 362 In the frame of a project for one of our Top Clients, we are seeking for a Regulatory Affairs Specialist ( pharmacist ) responsible for ensuring the delivery of regulatory activities performed onsite in Paris region. About us Group 10 Responsibilities Under the responsibility of the regulatory coordinator...

Regulatory Affairs Specialist 362 In the frame of a project for one of our Top Clients, we are seeking for a Regulatory Affairs Specialist ( pharmacist ) responsible for ensuring the delivery of regulatory activities performed onsite in Paris region. About us Group 10 Responsibilities Under the responsibility of the regulatory coordinator...

The Director, RA CMC Combination Products will work cross-functionally to lead development and implementation of global combination product/Medical Devices regulatory strategies across all applicable programs and lifecycle stages in accordance with program objectives. Advanced degree (eg MS, PhD) preferred. ~ Regulatory CMC experience in medical device and...

ABOUT THE JOBWant a 3D Career? Join Norgine.At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community. We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits. Bring everything about yourself that you’re proud of,...

ABOUT THE JOBWant a 3D Career? Join Norgine.At Norgine, our colleagues Dare themselves to be different and try new things, Drive to achieve their goals and beyond, and Develop themselves and their community. We call it the 3D career at Norgine and it offers you a fully-rounded experience with no limits. Bring everything about yourself that you’re proud of,...