Engineering Manager

Job description

Key Responsibilities1. Leadership & StrategyLead, mentor, and develop a team of system software and scripting engineers working on medical devices and associated infrastructure.Define the technical roadmap for system-level components, automation, configuration management, and OS hardening in alignment with product, quality, cybersecurity, and regulatory objectives.Collaborate closely with global R&D, Systems Engineering, QA/RA, Cybersecurity, IT, and Service to ensure cohesive end-to-end solutions.2. OS Component (Medical Devices)Oversee the development of OS components interfacing with hardware APIs, embedded subsystems, and ensuring seamless integration with system level componentsEnsure robust, reusable OTS / drivers that provide standardized access to hardware and system-level features while supporting safety, reliability, and cybersecurity requirements.Drive systematic maintenance and ensure backward compatibility, risk control, and alignment with design controls, change control, and quality processes.4. Documentation, Standards & Knowledge SharingEnsure comprehensive documentation of system-level components, APIs, scripts, Windows / Linux hardening baselines, GPOs, SCCM deployment configurations, and configuration procedures in accordance with design control and QMS requirements.Adhere to Zeiss medical SW development process and ensure the deliverables are in line with the established roadmap.Foster a culture of knowledge sharing via design reviews, training, and best-practice guidelines, ensuring cross-functional understanding of system behavior, Windows / Linux security baselines, and deployment processes.6. Governance, Quality, Compliance & CybersecurityDefine and enforce coding, configuration, OS hardening, cybersecurity, and documentation standards aligned with medical device regulations and internal QMS.Partner with QA/RA and Cybersecurity to support compliance with relevant standards and regulations (e.g., IEC 62304, ISO 14971, IEC 81001-5-1, ISO 27001, MDR/FDA expectations).Responsible for Lifecycle management for OS release across MED portfolio. Qualifications & ExperienceBachelor’s or master’s degree in computer science, Software Engineering, Electrical/Computer Engineering, or related field.Significant experience in system-level software development (e.g., C/C++, low-level APIs, OS internals, hardware interaction) and/or scripting (e.g., PowerShell, Bash, Python) in Windows and/or Linux.Proven experience leading or managing engineering teams, ideally in a regulated or safety-critical domain (preferably medical devices) including hiring activities.Experience working under a Quality Management System and with medical or comparable standards (e.g., IEC 62304, ISO 13485, ISO 14971, IEC 81001-5-1, ISO 27001 or similar).Foster a culture to establish efficient troubleshooting of complex system issues, performance optimization, and system hardening. Key Skills & CompetenciesStrong people leadership, coaching, and cross-functional collaboration skills.Deep understanding of Windows & Linux operating systems in medical device domain - networking, security, and system integration in a product context.Structured, risk-aware decision making with focus on patient safety, product quality, and regulatory compliance.Ability to review technical engagement with strategic planning, prioritization, and stakeholder management.Collaboration with the PO for low level backlog grooming and delivery to ensure optimum resource planning.