Senior Medical Device Specialist
Microsoft
Posted on May 3, 2025
Senior Medical Device Specialist
London, United Kingdom
Date posted
May 02, 2025
Job number
MIC014338
Work site
Microsoft on-site only
Role type
Individual contributor
Profession
Software Engineering
Discipline
Software Quality Engineering
Employment type
Full-time
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Job Description
Overview
Microsoft is dedicated to empowering healthcare organizations to achieve their goals and improve patient care.
We are looking to hire a Senior Medical Device Specialist, with a strong technical background and a customer-driven passion for regulatory work, to join our team. This is an opportunity to join a growing organization focused on healthcare-specific data platforms, AI products and Microsoft Cloud for Healthcare. We are looking for someone who will bring Medical Device and Regulatory expertise, with a focus on software to our team.
We are a team that believes in making a difference and bringing a positive approach to challenges. If you are looking for a team that will have an impact on an evolving society, provide a diverse workplace, and challenge you to learn and grow, our team may be the place for you.
Microsoft’s mission is to empower every person and every organization on the planet to achieve more. As employees we come together with a growth mindset, innovate to empower others, and collaborate to realize our shared goals. Each day we build on our values of respect, integrity, and accountability to create a culture of inclusion where everyone can thrive at work and beyond.
Responsibilities
- Ensure compliance with regulations governing Software Medical Devices including ISO 13485, ISO 27001, and ISO 62304, as well as support for the Quality Management System (QMS)
- Author technical documentation, and designs and implements Medical Device validation protocols for Software focused programs
- Conduct and contribute to Medical Device audits, working with engineering and PM teams to ensure robust regulatory oversight and documentation of the Medical Device program.
- Serve as a SME for Engineering and other organizations, proactively revising and developing Medical Device guidance materials for healthcare services.
- May apply cross-functional knowledge to other compliance programs.
- Embody our Culture and Values.
Required Qualifications:
- Experience in Software compliance product/technical program management OR equivalent experience.
- Experience writing technical documentation for Medical Devices or other regulated industries.
- Professional experience in a combination of roles in regulatory, quality, clinical evaluation, risk management, technical program management, or equivalent.
Preferred Qualifications:
- Advanced degree in Regulatory or Healthcare compliance.
- Experience of the healthcare regulatory landscape, including SaMD and device CDS for the United States and Medical Device Software for the European Union.
- Experience testing and validating software systems.
- Regulatory Affairs Certification (RAC) Devices, lead ISO13485 auditor, or equivalent.
- Experience working with legal / regulatory teams to translate regulatory and standard requirements to actionable engineering plans.
- Experience with consumer-focused software solutions.
Benefits/perks listed below may vary depending on the nature of your employment with Microsoft and the country where you work.
Industry leading healthcare
Educational resources
Discounts on products and services
Savings and investments
Maternity and paternity leave
Generous time away
Giving programs
Opportunities to network and connect
Microsoft is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age, ancestry, citizenship, color, family or medical care leave, gender identity or expression, genetic information, immigration status, marital status, medical condition, national origin, physical or mental disability, political affiliation, protected veteran or military status, race, ethnicity, religion, sex (including pregnancy), sexual orientation, or any other characteristic protected by applicable local laws, regulations and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application process, read more about requesting accommodations.