Senior Technical Product Manager
Leads definition and commercialization of next-generation medical devices, translating customer and clinical needs into product requirements and roadmaps. The role coordinates cross-functional engineering, clinical, manufacturing, quality, and regulatory teams throughout the product lifecycle.
About the job
Responsibilities
- Own product requirements, user needs, intended use, and system-level product definition for a major medical-device product line.
- Translate customer, clinical, technical, and business needs into product requirements, roadmaps, and development priorities.
- Partner with systems, hardware, firmware, software, algorithms, clinical, quality, regulatory, business development, operations, and manufacturing teams.
- Lead cross-functional tradeoff discussions covering functionality, usability, technical risk, manufacturability, regulatory requirements, cost, and schedule.
- Drive products through concept, feasibility, verification, validation, manufacturing transfer, commercialization, and sustaining engineering.
- Coordinate usability studies, customer evaluations, clinical feedback, and product validation activities.
- Support design controls, requirements traceability, risk management, design reviews, and regulatory documentation.
- Drive Agile product development practices across multiple initiatives and portfolios.
- Collaborate with suppliers, contract manufacturers, and external partners on development, manufacturing readiness, and launches.
- Communicate product status, decisions, risks, and roadmap updates to stakeholders and leadership.
Requirements
- Bachelor's degree in Engineering, Computer Science, Biomedical Engineering, Business, or a related field; an advanced degree is preferred.
- 5–8 years of experience in product management, systems engineering, device development, or related technical leadership roles.
- At least 3 years supporting development and commercialization of hardware, medical devices, wearables, or other multidisciplinary products.
- Experience translating customer, clinical, and business needs into requirements, roadmaps, and priorities.
- Experience working with hardware, firmware, software, systems, manufacturing, and quality teams across the product lifecycle.
- Experience with design controls, verification and validation, manufacturing transfer, and commercialization.
- Strong technical aptitude and ability to evaluate engineering tradeoffs involving functionality, usability, reliability, manufacturability, cost, and schedule.
- Strong communication, organizational, and stakeholder-management skills.
Nice-to-haves
- Experience in regulated industries, including medical devices, healthcare technology, or other safety-critical products.
- Experience with Ketryx, Jira, Figma, GitHub, Asana, or similar product-development and collaboration tools.
Compensation and Benefits
- Base salary range: $147,000–$167,000.
- Total compensation includes equity, paid time off, and other benefits.
Skills
Product Management, Medical Devices, Systems Engineering, Hardware, Firmware, Software Development, Design Controls, Requirements Traceability, Risk Management, Verification And Validation, Manufacturing Transfer, Agile, Jira, Figma, GitHub
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