Verification & Validation (V&V) Firmware Engineer

We are seeking an experienced Firmware Integration & Verification & Validation (V&V) Lead to support CT system development. In this role, you will drive firmware integration, lead V&V activities, and ensure alignment with quality and regulatory standards. You will work cross-functionally to manage technical execution, mitigate risks, and deliver high-quality solutions within defined timelines.This position requires strong leadership, hands-on technical expertise, and the ability to operate across hardware, firmware, and software domains in a regulated environment.Key ResponsibilitiesRepresent the Firmware team throughout the full design control lifecycle—from requirements definition and planning through product release.Lead integration strategy, including defining integration requirements and managing controlled integration across subsystems.Own end-to-end Verification & Validation (V&V) activities, including planning, execution, and reporting.Drive and support CI/CD pipelines and continuous testing frameworks to enhance development efficiency and product quality.Collaborate with cross-functional and global teams to identify and manage technical risks, dependencies, and design trade-offs.Ensure compliance with Quality Management System (QMS) requirements and support Design History File (DHF) documentation and release.Act as ALM administrator, enabling effective requirements management, traceability, and test execution.Troubleshoot and debug complex issues across hardware, firmware, and software layers.Provide clear technical documentation and communication to stakeholders.Required QualificationsBachelor's degree in STEM (Science, Technology, Engineering, Mathematics).10+ years of experience in firmware, systems integration, or V&V within complex environments.Strong background in hardware-software system integration, preferably in regulated industries such as medical devices (CT, MR, or similar).Proven leadership experience driving cross-functional technical initiatives.Hands-on experience with CI/CD, integration workflows, and test automation.Strong analytical and problem-solving skills with the ability to proactively mitigate risks.Experience with tools such as ALM, ClearQuest, Rally, or similar.Preferred QualificationsExperience working in global, distributed teams across multiple time zones.Familiarity with regulatory and compliance standards in medical device environments.Strong ability to influence stakeholders and drive strategic technical decisions.