Regulatory Submissions Associate

Job SummaryOur clinical operations activities are growing rapidly, and we are currently seeking a full-timeoffice-basedRegulatory Submissions Coordinator to join our Clinical Operations team inLyon. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Medpace, Inc. is looking for a full-time Regulatory Submissions Coordinator to join our Clinical Operations team in Lyon. This role is crucial for managing the clinical trial process and involves ensuring compliance with regulatory standards.The ideal candidate will have a Bachelor's degree in a Life Sciences field, with at least 4-5 years of relevant...

As a key member of the French Regulatory team, you will collaborate closely with local and regional regulatory colleagues to ensure compliance with French and EU regulations, maintain product registrations, and support the ongoing success of FMC's portfolio.ResponsibilitiesPrepare, review, amend, and update product labels for the French market, ensuring...

Developing innovative treatments for Human and Animal Health has been the commitment of Boehringer Ingelheim for more than 130 years. Boehringer Ingelheim is a family-owned company dedicated to research and development and ranks among the world’s top 20 pharmaceutical companies. Every day, our employees create value through innovation in the fields of...

Developing innovative treatments for Human and Animal Health has been the commitment of Boehringer Ingelheim for more than 130 years. Boehringer Ingelheim is a family-owned company dedicated to research and development and ranks among the world’s top 20 pharmaceutical companies. Every day, our employees create value through innovation in the fields of...

FMC Corporation's Regulatory team in France is seeking a detail-oriented regulatory professional to collaborate with local and regional colleagues to ensure compliance with French and EU regulations, maintain product registrations, and support the portfolio's ongoing success.You will prepare, review, and update labels and SDS, maintain regulatory databases,...

A DeepTech start-up in Lyon seeks a Quality and Regulatory Manager to maintain certifications and improve AI-powered medical devices. Experience with MDR 2017/745, regulatory submissions, and managing quality systems is essential. The role offers an exciting opportunity to contribute to obstetric ultrasound advancements in a startup environment. Fluency in...

Quality and Regulatory Manager M/F Get AI-powered advice on this job and more exclusive features. DIAGNOLY is a DeepTech start-up headquartered in Lyon, France. We are redefining obstetric and maternal-fetal medicine through real-time AI in ultrasound. We are looking for an experienced Quality and Regulatory Engineer who is ready for the challenge of...

With sales of €700m and 3,300 employees worldwide, Nemera is one of the leading global manufacturers of complex drug delivery systems for the pharmaceutical industry, offering to patients a broad product portfolio which includes inhalation devices, injection devices, nasal and dermal pumps and ophthalmic delivery devices. Nemera has built very long...