Nemera - France, Lyon, IT - Administration

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.

Lead Nemera's digital transformation in Lyon, driving smarter manufacturing through data and AI. You will manage the roadmap, deploy data platforms, and deliver value from BI initiatives. Requires 10+ years' experience, including scaling data use cases in industrial settings, and willingness to t...