Zimmer Biomet

About the Company

Zimmer Biomet is a global medical technology leader with a comprehensive portfolio designed to maximize mobility and improve health. We advance our mission to alleviate pain and improve the quality of life for patients around the world with our innovative products and suite of integrated digital and robotic technologies leverage data, data analytics and artificial intelligence. Founded in 1927 and based in Warsaw, Zimmer Biomet has operations in more than 25 countries and sales in more than 100 countries. We maintain world-class scientific facilities and resources and collaborate with leading clinicians and researchers around the world.

Awards and Recognitions
• Forbes Best-in-State Employers in Indiana (2020 and 2021)
• Newsweek’s America’s Most Responsible Companies (2021)
• Military Friendly Employer by VIQTORY (2019 and 2020)
• Best Employer Award: China (2011-2021)
• Great Place to Work: Brazil (2021)
• Indiana Manufacturers Association Manufacturing Excellence Awards (2020)
• ComputerWorld’s "Best Places to Work in IT" (2018-2020)
• Forbes Global 2000 (2020 and 2021)
• Fortune 500 List (2020 and 2021)

Listed Jobs

Company Name

Zimmer Biomet

Job Title

Ingénieur Software h/f

Job Description

**Job title** Software Engineer (Medical Devices) **Role Summary** Engineer responsible for the development, enhancement, and compliance of medical software dossiers and development environments within R&D. Works closely with consultants, quality, and regulatory teams to meet IEC, CFR, and MDR standards. **Expectations** - Proactive, detail‑oriented work with strong leadership and multidisciplinary coordination skills. - Fluent in English (minimum live level). - Minimum 5 years of proven experience in medical device software design, development, and validation. **Key Responsibilities** - Analyze and remediate existing software architecture. - Update design files in line with IEC 62304 and IEC 81001‑5‑1. - Modify code to support remediation activities. - Plan, execute, and document verification and validation tests to ensure integrity and compliance. - Collaborate with Quality and Regulatory Affairs to maintain accurate documentation. - Implement development‑specific tooling (tests, Git, CI/CD). - Participate in cross‑functional teams to maintain a robust development environment. **Required Skills** - Programming languages: Python, C, C++. - Windows development environment. - Knowledge of medical device software life‑cycle and cybersecurity fundamentals. - Familiarity with IEC 62304, IEC 81001‑5‑1, 21CFR Part 820, and MDR 2017/745. - Strong analytical, problem‑solving, and communication skills. **Required Education & Certifications** - Bachelor’s or Master’s degree in Engineering or equivalent software development field. - Relevant certifications (e.g., medical device software competency, IEC training) preferred but not mandatory.

Villeneuve-lès-bouloc, France

Hybrid

Mid level

26-01-2026