Senior Technical Product Manager (Software)

Edwards Lifesciences•Irvine, CA

1d•$121,000 - $171,000•Onsite

About The Position

Many structural heart patients suffer from heart failure with limited options. Our Implantable Heart Failure Management (IHFM) business's AI, Product and Platforms organization is at the forefront of addressing these unmet patient needs through pioneering technology that enables early, targeted therapeutic intervention. Our innovative solutions are not just transforming patient care but also creating a unique and exciting environment for our team members. It is our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey. At Edwards Lifesciences, the Implantable Heart Failure Management (IHFM) AI, Product and Platforms organization designs and builds the software and data products that clinicians and patients depend on. As a Senior Technical Product Manager, you co-own product strategy and roadmap with Marketing for a single product area, one application or one platform service area, translating the marketing requirements and writing the technical requirements yourself and partnering with engineering as a credible technical peer who can argue API design and architecture choices. Based in Irvine, CA, you'll join a high-impact medtech innovation hub in the heart of Orange County, collaborating in person with cross-functional teams to shape patient-focused technology.

Requirements

Bachelor's degree in Computer Science, Engineering, Information Systems, or a related field and 8 years of hands-on experience managing projects of increasing complexity, or equivalent work experience based on Edwards criteria.
Demonstrated experience owning product strategy and roadmap for a technical software product area, from discovery through shipped and measured outcomes.
Proven ability to author detailed, testable technical product and feature requirements, including acceptance criteria.
Sufficient technical depth to understand code, system designs, APIs, and architecture tradeoffs and effectively partner with engineering teams.
Strong knowledge of software design control practices in regulated environments, including 21 CFR 820.30, IEC 62304, and design change control.

Nice To Haves

Experience with regulated products (SaMD, medical devices, or another regulated domain) and design control practice.
A prior engineering background, or hands-on familiarity with the application and platform stack (APIs, cloud services, mobile or web).
Experience partnering with UX Design and Marketing Product Management on shared product decisions.
Familiarity with product analytics instrumentation and experimentation.

Responsibilities

Co-own product strategy and roadmap with Marketing for a single product area (one application or one platform service area), from problem definition through shipped, measured outcomes.
Personally, author detailed technical product requirements with appropriate specificity, and participate substantively in architecture reviews.
Own the calls within your area: feature build vs. tech debt, depth vs. breadth, refactor vs. ship.
Measure results through both business metrics (adoption, retention, conversion) and technical metrics (latency, reliability, defect rate).
Partner closely with engineering tech leads as a peer who argues architecture, not just a stakeholder who files tickets.
Run customer discovery and synthesize feedback and product analytics into roadmap decisions, using tools such as Productboard, Pendo, Dovetail, and Amplitude.
Author requirements that stand as software design inputs under 21 CFR 820.30(c) and IEC 62304, with acceptance criteria that become verification criteria for regulated products.