Descrizione dell'offerta
Experteer Overview
In this role you will strengthen the secure software development life cycle for diagnostic instruments at a global leader in healthcare technology. You’ll work with cross‑functional teams to define and implement security requirements, manage vulnerability activities, and coordinate with third‑party partners and regulatory bodies. Your work directly supports product quality and patient safety while enabling secure, compliant devices. This is a hands‑on, impact‑driven position in a fast‑growing, global context. Retribuzione / Benefits
Define and update software security requirements derived from higher‑level needs, market feedback, or regulatory demands Manage vulnerability scans, penetration tests, and SBOM monitoring; integrate findings into the security framework Develop and review internal security testing plans and support their execution Contribute to the release and deployment of software security updates Collaborate with third‑party partners on security findings and information requests Communicate security outcomes to notified bodies and regulatory agencies (e.g., FDA) Coordinate with other development areas, Project Management, and Device Lead on joint tasks Troubleshoot and support bug fixing; share expertise across functions Provide team knowledge and problem‑solving support across the organization Responsabilità
Master's Degree in specified fields Previous experience in a similar role Experience in IVD and/or highly regulated FDA environments is appreciated Knowledge of SW Life Cycle (EN 62304) and cybersecurity principles Understanding of authentication, authorization, auditing, hardening, and data integrity Requisiti fondamentali
Competitive salary and benefits package Hybrid work Global collaboration Equal opportunity employer
#J-18808-Ljbffr
In this role you will strengthen the secure software development life cycle for diagnostic instruments at a global leader in healthcare technology. You’ll work with cross‑functional teams to define and implement security requirements, manage vulnerability activities, and coordinate with third‑party partners and regulatory bodies. Your work directly supports product quality and patient safety while enabling secure, compliant devices. This is a hands‑on, impact‑driven position in a fast‑growing, global context. Retribuzione / Benefits
Define and update software security requirements derived from higher‑level needs, market feedback, or regulatory demands Manage vulnerability scans, penetration tests, and SBOM monitoring; integrate findings into the security framework Develop and review internal security testing plans and support their execution Contribute to the release and deployment of software security updates Collaborate with third‑party partners on security findings and information requests Communicate security outcomes to notified bodies and regulatory agencies (e.g., FDA) Coordinate with other development areas, Project Management, and Device Lead on joint tasks Troubleshoot and support bug fixing; share expertise across functions Provide team knowledge and problem‑solving support across the organization Responsabilità
Master's Degree in specified fields Previous experience in a similar role Experience in IVD and/or highly regulated FDA environments is appreciated Knowledge of SW Life Cycle (EN 62304) and cybersecurity principles Understanding of authentication, authorization, auditing, hardening, and data integrity Requisiti fondamentali
Competitive salary and benefits package Hybrid work Global collaboration Equal opportunity employer
#J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
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