Les missions du poste 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 lasting, strong relationships with the leading global pharmaceutical companies globally by providing high quality development, industrialization and manufacturing services. Nemera develops and manufactures its own IP product platforms but also offers also fully custom developments and contract manufacturing. Nemera's manufacturing sites are located in the US, France, Germany, Brazil and Poland. The headquarters and Innovation Center for early device design and development are located in France (Lyon). We have big ambitions at Nemera! We are growing our franchises and strengthening our capabilities. We are currently looking for passionate people ready to make a difference in the following open position: Regulatory Affairs Manager F/M/X, based in Lyon (7e). Within Nemera's headquarters, you will lead the Regulatory & Compliance activities for a diverse portfolio of ENTD (Ear, Nose, Throat & Dermal), Ophthalmic and Inhalation medical devices and combination products, covering different regulatory pathways and risk profiles. You will report to the Global Regulatory & Compliance Manager, and work in close collaboration with development, quality, industrialisation, operations and commercial teams, as well as with customers and external stakeholders. You will be involved throughout the full product lifecycle, from early development phases to post-market activities, defining regulatory strategies, supporting quality management plans and contributing to QMS development and continuous improvement. Job Description : - You will manage the Regulatory & Compliance team of the Business Units ENTD and Ophthalmic and
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