Senior Knowledge Specialist, GMA
12 ore fa
Italia
UL Solutions
Tempo pieno
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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. Responsibilities Demonstrate the ability to complete core daily tasks cross multiple regulations, countries, such as:- Publishing high-quality news and delivering accurate and valuable research report with a high level of quality and within required timelines
- Maintaining data
- Updating relevant internal files trackers and related resources
- FDA Cybersecurity Requirements for Medical Devices
- EU Medical Device Regulation (MDR) cybersecurity expectations
- ISO 14971 cybersecurity considerations
- Cyber Resilience Act (CRA)
- NIS2 Directive
- AI Act cybersecurity requirements
- FDA Premarket & Postmarket Cybersecurity Guidance
- IMDRF Cybersecurity Frameworks
- Health software and Software as a Medical Device (SaMD) requirements, etc.
- 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.
- Experienced and knowledgeable for one or multiple geographic area, multiple areas of regulations and lead business decisions from COUs and other team members.
- 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.
- Bachelor’s Degree Engineering, Biomedical Engineering, Computer Science / Software Engineeri