Nemera - France, Lyon, On-site work

Lead regulatory & compliance projects for drug delivery devices at Nemera's Lyon HQ. You will define strategies and manage submissions (eCTD, CE, MDR) from design to post-market. Requires 5+ years in pharma/biomed, expertise in ISO 13485, 21 CFR Part 820, and GMP within a transversal role.

Join Nemera in Lyon as a Simulation Engineer to develop innovative drug delivery solutions. You will model and analyze components using FEA tools like MSC Software and SolidWorks. We seek a mechanical engineering graduate fluent in English/French, skilled in simulation, Python, and supplier relat...