Overview
This is a product security role with a global scope, partnering across sites in Ireland, Austria, and Germany. The role blends technical expertise and business engagement—about 70–80% of time will be spent collaborating directly with external clients and internal stakeholders.
What You’ll Do
* Conduct product security risk assessments, prepare reports, and present findings to clients and internal teams.
* Partner with R&D to ensure secure architecture, coding practices, and compliance with medical device security standards.
* Support vulnerability management, remediation planning, and security documentation processes.
* Act as a liaison between clients, the MSS team, and the Product Security organisation—gathering, analysing, and relaying security-related requirements.
* Guide teams on encryption, authentication, audit logging, patch management, and other core security measures.
Qualifications
* 3–5 years’ experience in IT Security, Cybersecurity, or secure software development—ideally in medical devices, pharma, or another regulated industry.
* Strong client-facing skills and experience in stakeholder management.
* Knowledge of regulatory compliance (e.g., FDA, MDR) and security standards.
* Understanding of embedded device security, network security fundamentals, and secure coding practices.
* Experience creating technical documentation for software products.
* Security certifications (CISSP, CASP+, CSSLP) are a plus.
Seniority level
* Associate
Employment type
* Full-time
Job function
* Information Technology
Industries
* Software Development
* Medical Practices
* Medical Equipment Manufacturing
Location: Limerick
Hybrid: 3 days in the office
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