Technical Program Manager

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Q Bio

πŸ’΅ $180k-$250k
πŸ“Remote - United States

Summary

Join Q Bio as a Technical Program Manager to lead the development and execution of innovative medical technology programs. You will collaborate with engineering, data science, regulatory, and manufacturing teams to deliver cutting-edge medical imaging solutions. Responsibilities include coordinating large-scale projects, developing comprehensive program plans, defining program scope and requirements, leading design reviews, and driving the end-to-end product lifecycle. You will manage cross-functional teams, establish a quality-first culture, and maintain a program-level risk management process. The role requires strong leadership, analytical, and communication skills, along with experience in a regulated environment and SaMD development. Q Bio offers a competitive compensation and benefits package and the opportunity to work on impactful medical technology.

Requirements

  • Bachelor's degree in Engineering, Computer Science, or related technical field; Master's or equivalent work experience in Healthcare or related fields is preferred
  • 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
  • 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

Responsibilities

  • Coordinate a large, multisite project to prototype and validate Q Bio's 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

Benefits

  • 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
  • $180,000 - $250,000 a year

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