UL Solutions

Senior Medical Device Cybersecurity Specialist – EU Regulations

In short

This role builds and maintains deep expertise in global medical device cybersecurity regulations (FDA, EU MDR, Cyber Resilience Act, NIS2, EU AI Act, ISO 14971, IMDRF), producing regulatory intelligence, research reports, training, and advisory support for customers and internal teams. The employer is a testing, inspection and certification (TIC) company expanding knowledge services in cybersecurity, AI, data governance, and connected health technologies. It requires 5-7 years of relevant experience, a bachelor's degree in engineering, computer science, biomedical engineering or related field, strong regulatory/customer-facing communication skills, and program management ability.

About the Role
You are responsible for developing and maintaining deep expertise in global medical device cybersecurity regulations, standards, guidance documents, and conformity assessment requirements. The individual will monitor regulatory changes, interact with authorities and industry stakeholders, contribute to business growth initiatives, lead complex research projects, represent GMA as a cybersecurity knowledge leader, and provide advisory support for customer engagements related to regulatory compliance and market access.
The role drives the creation of regulatory intelligence content, customized research studies, training materials, customer-facing reports, and strategic insights covering cybersecurity requirements across regions including North America, Europe, Asia-Pacific, Latin America, and the Middle East, etc.
This position also contributes to the expansion of GMA knowledge services in cybersecurity, artificial intelligence, data governance, connected health technologies, software as a medical device (SaMD), and emerging digital health regulations. The individual is expected to build strong relationships with authorities, industry associations, and internal technical experts to strengthen UL's market leadership in medical cybersecurity services.
In this role, you'll help organizations navigate the evolving world of medical device cybersecurity, AI, and digital regulations. You'll turn complex regulatory requirements into clear, practical insights for customers and internal teams.
Responsibilities
•Research and monitor global medical device cybersecurity regulations, standards, guidance, and industry trends.
•Publish high-quality regulatory news, research reports, executive summaries, impact assessments, and comparison reports.
•Provide clear guidance on regulatory requirements, certification pathways, and compliance expectations.
•Develop and deliver internal and external training on medical device cybersecurity requirements.
•Build expertise across key regulations and frameworks, including:
•FDA medical device cybersecurity requirements and guidance
•EU Medical Device Regulation (MDR)
•Cyber Resilience Act (CRA)
•NIS2 Directive
•EU AI Act
•ISO 14971
•IMDRF cybersecurity frameworks
•Health software and Software as a Medical Device (SaMD) requirements
•Support customers and internal teams with regulatory questions and local market acceptance topics.
•Mentor and provide technical guidance to colleagues, sharing knowledge and best practices.
•Partner with business development teams to identify new opportunities and support customer proposals.
•Help develop regulatory intelligence services and subscription-based knowledge offerings.
•Contribute to emerging areas such as cybersecurity, AI, data governance, and new technology regulations.
•Maintain accurate and up-to-date regulatory information within internal knowledge tools, databases, and trackers.
•Follow company standards for ethics, physical security, and digital security.
•Support other projects and responsibilities as needed.
Requirements
•Bachelor's Degree in Engineering, Biomedical Engineering, Computer Science / Software Engineering, Medical Device Cybersecurity or Information Security or other specialization based on the specific coverage.
•Minimum 5-7 years of relevant experience.
•Excellent working knowledge of the TIC business and the industries in which the business functions. Independently able to connect the regulation rules with customer needs and business opportunities.
•Natural influencing skills, confidence and ability to deliver the message.
•Good planning, organization and project management skills. Earlier program management experience preferred.
•Able to deal with ambiguity and take decisions, support customers in understanding their problem and provide valid solutions based on knowledge of schemes and past experiences.
•Strong customer focus and solution-oriented mindset.
•Excellent communication skills, able to summarize requirements and describe difficult concepts in easy words, network builder.
•Excellent written and verbal communication skills in English.
Total Rewards
The salary range for this position in Italy is 45,000 EUR to 55,000 EUR, based on multiple factors including job-related knowledge/skills, experience, geographical location, and other factors. This position is eligible for an annual bonus with a target payout of 10% of base salary. You'll also enjoy annual paid leave, access to ULS University to support continuous learning and career growth, two volunteering days each year to participate in community activities, and flexible working arrangements designed to help you balance work and life.

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