Job Description

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, contributes to business growth initiatives, and 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.

• 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.
• Bachelor’s Degree 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 be able to deliver the message.
• Good planning, organization and project management skills. Earlier program management experience preferred.
• Able to deal in the 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 in communication, able to summarize requirements and describe with easy word difficult concept, network builder.
• Excellent written and verbal communication skills in English.

Total Rewards: We understand that rewards are an important consideration as you plan the next step in your career. The salary range for this position in Italy is 45000EUR to 55000EUR and is 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 our 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.

Disclaimer: This role is gender-neutral and open to all qualified applicants, regardless of gender identity or expression

A global leader in applied safety science, UL Solutions (NYSE: ULS) transforms safety, security and sustainability challenges into opportunities for customers in more than 110 countries. UL Solutions delivers testing, inspection and certification services, together with software products and advisory offerings, that support our customers’ product innovation and business growth. The UL Mark serves as a recognized symbol of trust in our customers’ products and reflects an unwavering commitment to advancing our safety mission. We help our customers innovate, launch new products and services, navigate global markets and complex supply chains, and grow sustainably and responsibly into the future. Our science is your advantage.