271 france English-speaking jobs in Lyon

Lead development of Core Lab Systems (Medical Imaging, Cardiovascular, Biosensor Tech) as Product Manager (Research Engineer). Drive strategy, manage end-to-end execution using Agile, and translate user needs into requirements.

Define the long-term technical vision for Malt's platform, driving backend (Kotlin/Java), frontend (Nuxt/VueJS), and GCP infrastructure. Architect foundations and pioneer agentic workflows to multiply engineering output.

Senior Software Platform Engineer to improve Developer eXperience and lower technical overhead. Build tools, IaC, and libraries to support cross-team productivity. English is mandatory.

Scaleway proudly serves thousands of customer across the private and public sector, from corporations like France

Norwegian multinational that values collaboration and innovation.This role can be based in Norway, France

Job title: Scientific Data Analyst Location: France, Marcy l'etoileJob type : CDI Permanent Contract

Information Systems Management, Information Security or equivalent experience.CompanyAWS EMEA SARL (France

Company AWS EMEA SARL (France Branch) Job ID: A3124454 #J-18808-Ljbffr

This is a flexible role based in Gothenburg (Sweden), Ghent (Belgium), Wroclaw (Poland) or Lyon (France

This role is based in Amsterdam, Netherlands or in Lyon, France.

12 months Job Posting Aug 14, 2026, 4:04:38 PM Closing Date Sep 5, 2026, 4:59:00 AM Primary Location France-Lyon

This role involves clinical evidence generation, Post-Market Surveillance (PMS), and Post-Market Clinical Follow-Up (PMCF) for medical devices. Responsibilities include maintaining CERs, managing PMS activities, and ensuring EU MDR compliance.

R&D Preclinical Specialist focusing on Biocompatibility and Cytotoxicity for medical device development. This role involves creating BEPs/BERs per ISO 10993, conducting biological safety assessments, and analyzing cytotoxicity studies for dental biomaterials.

R&D Preclinical Specialist focusing on Biocompatibility and Cytotoxicity for medical devices. Develop BEPs/BER in ISO 10993, conduct biological safety assessments, and manage regulatory documentation for dental biomaterials. Requires Master's/PhD and 5+ years of relevant experience.

This role involves clinical evidence generation, Post-Market Surveillance (PMS), and PMCF programs for medical devices. Responsibilities include maintaining CERs, PSURs, and technical documentation under EU MDR.

Guest Experience Specialist assists clients with planning details, reservations, and service requests. The role requires clear communication, careful coordination, and dependable follow-up to ensure a positive experience. Key skills include strong customer service and organization.

Senior Python Data Scraping Engineer needed for the Tendem project. Drive specialized data scraping workflows using Python, BeautifulSoup, Selenium, and tools like Apify. Expertise in complex web extraction, data cleaning, and handling dynamic content is required.

Competitive Programming Expert needed to build problems and graders for AI coding models. Tasks include writing algorithmic problems, correct/incorrect solutions in C++/Python, and designing robust test cases. Strong CP background and C1+ English are required.

Manages regulatory compliance for pharmaceutical, medical device, or healthcare product development, approval, and marketing. Prepares and submits regulatory filings, liaises with agencies, and provides guidance to cross-functional teams.

Experienced Clinical Writer needed to lead high-quality clinical documentation for medical devices. Responsibilities include authoring development plans, clinical reports, and PMCF plans while ensuring regulatory compliance. Requires deep knowledge of medical device regulations and advanced English.