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Zimmer Biomet

Zimmer Biomet

www.zimmerbiomet.com

2 Jobs

17,850 Employees

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 background Company brand
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
Company background Company brand
Company Name
Zimmer Biomet
Job Title
Internal Audit Director
Job Description
**Job Title:** Internal Audit Director **Role Summary:** Senior internal audit executive responsible for leading a global audit team, designing and executing the annual audit plan, ensuring compliance with regulatory frameworks (SOX, ERM, cybersecurity, data privacy), and providing strategic risk insights to improve governance and operational efficiency. **Expectations:** - Deliver high‑quality audit services that align with corporate strategy and regulatory requirements. - Maintain a balanced risk-based audit plan and manage portfolio of engagements. - Provide objective, data‑driven recommendations to senior leaders. - Foster continuous improvement and process automation within the audit function. - Build and retain a high‑performing audit team. - Drive change management and transformation initiatives across the organization. **Key Responsibilities:** - Lead, mentor, and develop an international team of 8–10 auditors. - Own the annual risk assessment process, audit planning, and execution schedule. - Define audit procedures, conduct tests, and assess control effectiveness across financial, operational, and IT domains. - Prepare, review, and present audit reports, findings, and recommendations to management and the Audit Committee. - Design and implement continuous monitoring and advanced data analytics programs. - Manage SOX compliance, ensuring accurate risk assessments, control documentation, testing, and deficiency reporting. - Collaborate with Legal, Compliance, and IT to investigate and resolve compliance issues. - Monitor remediation progress and advise on control design for new systems/processes. - Develop dashboards and metrics for audit performance and provide reports to executive and board committees. - Participate in cross‑functional business initiatives (ERM, cybersecurity, business continuity, data privacy) to strengthen risk posture. **Required Skills:** - Proven leadership of audit teams with strong interpersonal and influence skills. - Strategic thinking and the ability to set clear departmental direction. - Deep knowledge of internal audit standards, SOX, ERISA, NIST, ISO, and industry‑specific regulations. - Strong analytical, data‑analytics, and risk‑assessment capabilities. - Excellent written and verbal communication, including report writing and presentations. - Ability to prioritize multiple engagements and meet tight deadlines. - Knowledge of automation, process improvement, and change management. - High ethical standards, sound judgment, and business acumen. **Required Education & Certifications:** - Bachelor’s degree in Accounting, Finance, Business Administration, or related field (Master’s preferred). - Certified Public Accountant (CPA) or Certified Internal Auditor (CIA) is required. - Additional certifications such as Certified Information Systems Auditor (CISA) or Certified Fraud Examiner (CFE) are advantageous.
United kingdom
Remote
04-02-2026