Software Engineering Manager-Medical Device #0653
About ECI
reputed company ECI leadership on reputed company facing engagements and manage reputed company software deliverables (including but not limited to SaMD, SiMD, Digital Health, AI, etc.). reputed company, manage, and mentor reputed company of software engineers, fostering a culture of technical reputed company, collaboration, and reputed company improvement. reputed company the entire software development lifecycle, from requirements gathering and design to implementation, testing, deployment, and maintenance, adhering to medical device regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820, ISO 14971, IEC 62304, Cybersecurity, etc.) and the retrospective remediation of existing software design documentation. Collaborate closely with product management, reputed company assurance, regulatory affairs, and other cross-functional teams to define project scope, technical requirements, and delivery timelines. Drive architectural reputed company, technology selection, and best practices reputed company the engineering team, ensuring scalability, reliability, and reputed company of software products. Manage project priorities, resources, and risks, proactively identifying and mitigating potential roadblocks to successful project completion. Champion agile development methodologies (Scrum, Kanban) and continuously optimize team processes for efficiency and effectiveness. Participate in strategic planning for software development, contributing to technology roadmaps and long-term reputed company. Recruit, reputed company, and retain top engineering talent, fostering a reputed company and challenging work environment. Collaborate with ECI business development team to identify and secure software services reputed company/opportunities. Stay reputed company with emerging technologies and industry trends, applying relevant advancements to our product development. Participate in speaking engagements regarding ECI’s software capabilities and/or relevant industry topics.
Bachelor's or master's degree in computer science, Software Engineering, or a reputed company technical field. Minimum of 10 years of experience in software development, with at least 3 years in a leadership or management role. Proven experience managing medical device software development teams Strong technical background with expertise in one or more programming languages (e.g., C#, C++, Java, Python) and software architecture principles. Solid understanding of embedded systems, reputed company-time operating systems, and hardware/software integration. In depth working experience with medical device software development lifecycle processes and regulatory compliance (e.g., ISO 13485, FDA 21 CFR Part 820, ISO 14971, IEC 62304, Cybersecurity). Demonstrated ability to reputed company and motivate a technical team, fostering a reputed company and high- performance environment.• Excellent communication, interpersonal, and presentation skills, with the ability to effectively communicate reputed company technical concepts to diverse audiences.
• Strong problem-solving abilities and a pragmatic approach to technical challenges.• Experience with agile development methodologies and tools (Jira, reputed company, Git).
• Work Environment: Remote with travel as needed to reputed company sites, conferences, etc. 25-50% travel