As a Technical Program Manager at Q Bio you will lead the development and execution of our innovative medical technology program. You will work cross-functionally with engineering data science regulatory and manufacturing teams to deliver breakthrough medical imaging solutions that meet strict quality and compliance standards while driving our mission forward.
What You Will Do
Coordinate a large multisite project to prototype and validate Q Bios proprietary approach to whole body quantitative MRI (qMRI)
Develop and execute comprehensive program plans for medical imaging technology managing the full lifecycle from concept to FDA 510(k) clearance
Define program scope system requirements schedules and deliverables for cross-functional teams and third-party partners
Lead system design reviews technical deep dives and trade-off studies to optimize designs for risk reduction and cost efficiency
Drive the end-to-end product lifecycle including product roadmap development features definition risk mitigation testing and submission all within an ISO 14385 compliant quality system (e.g. IEC 62304)
Facilitate collaboration between Mechanical/Electrical Engineering Data Science Software and Magnetics teams through critical design reviews
Manage system-level releases encompassing hardware software AI algorithms robotic components firmware and control systems
Drive program execution and coordinate activities across remote cross-functional internal team and external consultant teams of 25-30 professionals involved in a program
Establish a quality-first culture integrating compliance with FDA and international standards in team workflows and practices
Maintain a program-level risk management process covering regulatory technical and operational risks (identification assessment mitigation tracking)
Continuously assess product performance and feedback incorporating findings into iterative development cycles to improve user experience safety and compliance outcomes
What You Will Bring
Education
Bachelors degree in Engineering Computer Science or related technical field; Masters or equivalent work experience in Healthcare or related fields is preferred
Experience:
7 years of technical program management experience in a regulated environment with at least 3 years in Software as a Medical Device (SaMD) development. Open to candidates who have made a change in the last few years such as transitioning from engineering to PM or a similar role
Skills & Competencies:
Demonstrated success leading programs for SaMD from concept to post-market monitoring with particular experience with class II digital health products in US
Strong familiarity with regulatory submissions risk management and product validation processes in the medical device and digital health space
Strong understanding of medical imaging technologies preferably MRI systems
Experience managing cross-functional teams including software hardware and data science professionals
Solid understanding of software product lifecycle management and relevant guidelines and standards including ISO 13485 ISO 14971 and IEC 62304.
Experience with clinical trials and/or real-world evidence collection and how to integrate clinical data into product development
Excellent leadership skills with proven ability to manage remote technical teams
Strong analytical and problem-solving skills for conducting trade-off studies and risk assessments
Outstanding communication and stakeholder management abilities
What We Offer
Opportunity to work on cutting-edge medical imaging technology with real-world impact
Collaborative environment with top talent in engineering data science and healthcare
Competitive compensation and benefits package
Opportunity to help scale a start-up business and to professionally grow in a dynamic learning and development environment
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