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Strong brand, common managerial title, and likely metro location drive high applicant competition.
Regulatory, medical device, and embedded/desktop experience requirements make backgrounds less transferable across industries.
Role requires regulated-medical-device experience, specific desktop/embedded tech, and leadership, so filters will be strict.
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Lead multiple software engineering functions including Development and Test to deliver regulated medical device software products with predictable delivery and compliance.
Collaborate cross-functionally to align technical direction with product roadmaps, quality, and regulatory standards for connected medical devices and desktop applications.
Provide people leadership, technical guidance, and organizational development to engineering teams, ensuring engineering excellence, quality, and continuous improvement.
Experience managing software engineering teams in regulated industries such as medical devices, healthcare, life sciences, automotive, aerospace, or industrial automation.
Proven track record delivering software for desktop applications (e.g., Windows-based frameworks) and connected medical devices or real-time data systems.
Knowledge of regulatory standards and quality systems like FDA, ISO 13485, IEC 62304, ISO 14971, and cybersecurity for connected medical devices.
Work Experience Required: Not explicitly mentioned in the JD.
Experienced leader able to balance technical strategy with execution, managing cross-functional Agile teams in complex regulated environments.
Strong collaborator with stakeholders in Product Management, Quality, Regulatory, and Systems Engineering to drive integrated product development and compliance.
Data-driven manager focused on engineering metrics, team health, talent development, and predictable delivery in fast-paced, multi-priority settings.