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Tier-1 brand, metro location, and mid-level experience increase applicant competition.
Core security engineering skills transfer across industries, but medical-device regulatory expertise increases specificity.
Explicit 5–7 years, degree requirement, and specialized security/regulatory skills make filters strict.
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Lead security risk assessments and threat modeling throughout the product development lifecycle for medical device products.
Plan and execute security testing (penetration testing, vulnerability assessments, secure code reviews) and manage vulnerability remediation.
Develop and integrate security automation tools and support compliance with medical device cybersecurity standards and regulations.
Bachelor's or Master's degree in Computer Science, Cybersecurity, Software Engineering, Electronics Engineering, Information Security, or related field.
5–7 years of experience in Product Security, Application Security, Cybersecurity Engineering, or Medical Device Security.
Experience securing connected products, embedded systems, desktop apps, cloud services, or IoT platforms.
Proficiency in Python programming; experience with security tools like Burp Suite, OWASP ZAP, and knowledge of medical device cybersecurity regulatory standards (FDA Cybersecurity Guidance, IEC 62304, NIST frameworks).
Experienced in regulated medical device or healthcare product security environments.
Able to lead integrated security risk assessments and collaborate cross-functionally with development teams.
Skilled in automating security testing and integrating security into CI/CD and DevSecOps pipelines.