Lyon-Based Regulatory Program Lead – Medical Devices

Regulatory & Compliance Project Manager F / M / X (CDI) – Based in Lyon (7e). Job Description We are looking for a unique person ready to make a difference and join our Compliance & Regulatory team as Regulatory & Compliance Project Manager based in Lyon. Within Nemeras headquarters you will lead the regulatory & compliance design projects of drug delivery...

Job Summary: Our clinical operations activities are growing rapidly and we are currently seeking full-time, Regulatory Submissions Technical Advisors to join our Site Activation and Maintenance team, within Clinical Operations. This role will be office based in Lyon with flexibility to work from home. This position plays a key role at Medpace, preparing...

A mid-size CRO specializing in medical devices is seeking a Medical Writer focused on Clinical Evaluation to join their team in Lyon, France. This role involves developing clinical evaluation documentation for implantable medical devices and requires a university degree in life sciences or biomedical engineering, along with at least 2 years of experience in...

**Company Description** With sales of €600m and 3000 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...

About the Job Join Excelya, whereAudacity, Care, and Energydefine who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are currently looking for a Medical Writer focused on Clinical Evaluation for Medical Devices to join our growing team. This...

About The Job Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand. We are currently looking for a Medical Writer focused on Clinical Evaluation for Medical Devices to join our growing team. This...

Role DescriptionLine management, training of colleaguesEstablish and implement regulatory strategies ensuring new and existing products comply with the latest global requirements.Training the team with EMEA / FDA requirementsQualificationsMin 8 years in regulatory affairs in medical deviceMin 4 years as Regulatory Affairs ManagerExperience with EMEA / FDA...

**Location : Lyon, France** About ARCHIMED With offices in US, Europe and APAC ARCHIMED is a leading investment firm focused exclusively on the healthcare industries. Its mix of operational, medical, scientific and financial expertise allows the ARCHIMED team to serve as both a strategic and financial partner to European and North American small and...

Contract Opportunity: Manufacturing Engineer - Medical Devices (ISO 13485)Location: Lyon, FranceContract Duration: 12 monthsStart Date: ImmediateEngagement Type: FreelanceA leading medical device manufacturer is seeking an experienced Manufacturing Engineer to support advanced production operations in compliance with ISO 13485 and EU MDR standards. This is a...

What We Will Accomplish TogetherAlsinova, asubsidiary of the Astek Group, is a consulting firm specialized inLife Sciences. We support pharmaceutical, biotech, and medtech companies by providing high-level expertise inregulatory affairs, clinical development, data, quality, and pharmacovigilance. To support one of our major partners in thein vitro...