Regulatory Affairs Manager – Submissions

Approach People Recruitment is seeking a Regulatory Affairs Manager to lead regulatory strategies for pharmaceutical, medical device, or healthcare products. You will collaborate with R&D, Clinical, QA and Marketing to ensure full compliance throughout the product lifecycle.You will prepare submissions (INDs, NDAs, 510(k)s, PMAs) and liaise with FDA, EMA and...

Job Description: As a Regulatory Affairs Manager, you will be responsible for ensuring compliance with regulatory requirements related to the development, approval, and marketing of pharmaceutical, medical device, or other healthcare products. You will work closely with cross-functional teams to navigate the complex regulatory landscape and to ensure that...

Nemera, based in Lyon, seeks a Regulatory Affairs Manager to lead regulatory and compliance activities across ENTD, Ophthalmic and Inhalation devices. You will report to the Global Regulatory & Compliance Manager and collaborate with development, quality, and operations teams to ensure regulatory readiness throughout product lifecycles.You will build...

Nemera Department: Global Quality & RegulatoryCompany DescriptionWith 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...

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...

Nemera, a leading global medical device manufacturer, is seeking a Regulatory Affairs Manager based in Lyon (7e). You will lead Regulatory & Compliance activities for ENTD, Ophthalmic and Inhalation products, shaping regulatory strategies across EU, US and Canada.You will collaborate with development, quality, logistics and commercial teams, supervise a...

DAVRICOURT recherche un Manager Réglementaire et Conformité pour un portefeuille de dispositifs médicaux sur site à Lyon. Vous piloterez les activités réglementaires et assurerez la conformité tout au long du cycle de vie produit, en lien étroit avec les équipes développement, qualité et industrialisation.Vous avez 8 années d'expérience et une...

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...