Edwards Lifesciences Corp

Senior Technical Product Manager (Software)

Edwards Lifesciences Corp$121K — $171K *
Healthcare
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Computer Science, Engineering, Information Systems, or a related field with 8 years of experience.
  • Proven experience owning product strategy and roadmap for technical software products.
  • Ability to write detailed, testable technical product requirements with acceptance criteria.
  • Technical depth to understand code, system designs, APIs, and architecture decisions.
  • Strong knowledge of software design control practices in regulated environments.

Responsibilities

  • Co-own product strategy and roadmap with Marketing from problem definition to measurable outcomes.
  • Author detailed technical product requirements and participate in architecture reviews.
  • Make prioritization decisions between feature development and tech debt.
  • Measure product outcomes through business and technical metrics.
  • Partner with engineering leads as a credible technical peer regarding architecture.
  • Conduct customer discovery and synthesize feedback into roadmaps using analytics tools.
  • Author design requirements that comply with regulatory standards.

Benefits

  • Competitive salaries and performance-based incentives.
  • Wide variety of benefits programs catering to diverse individual needs.
Full Job Description
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.

How you'll make an impact
  • Product strategy and roadmap. Co-own strategy and roadmap with Marketing for a single product area (one application or one platform service area), from problem definition through shipped, measured outcomes.
  • Requirements, written yourself. Personally, author detailed technical product requirements with appropriate specificity, and participate substantively in architecture reviews.
  • Prioritization tradeoffs. Own the calls within your area: feature build vs. tech debt, depth vs. breadth, refactor vs. ship.
  • Outcomes, measured. Measure results through both business metrics (adoption, retention, conversion) and technical metrics (latency, reliability, defect rate).
  • Technical partnership. Partner closely with engineering tech leads as a peer who argues architecture, not just a stakeholder who files tickets.
  • Discovery and evidence. Run customer discovery and synthesize feedback and product analytics into roadmap decisions, using tools such as Productboard, Pendo, Dovetail, and Amplitude.
  • Design control. 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.


What you'll need (Required):
  • 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.


What else we look for (Preferred):
  • 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.


Aligning our overall business objectives with performance, we offer competitive salaries, performance-based incentives, and a wide variety of benefits programs to address the diverse individual needs of our employees and their families.

For California (CA), the base pay range for this position is $121,000 to $171,000 (highly experienced).

The pay for the successful candidate will depend on various factors (e.g., qualifications, education, prior experience). Applications will be accepted while this position is posted on our Careers website.

About Edwards Lifesciences Corp

Edwards Lifesciences is an American medical technology company headquartered in Irvine, California, specializing in artificial heart valves and hemodynamic monitoring. It developed the SAPIEN transcatheter aortic heart valve made of cow tissue within a balloon-expandable, cobalt-chromium frame, deployed via catheter. The company has manufacturing facilities at the Irvine headquarters, as well as in Draper, Utah; Costa Rica; the Dominican Republic; Puerto Rico; and Singapore; and is building a new facility due to be completed in 2021 in Limerick, Ireland.
Learn more about Edwards Lifesciences Corp
Size
15,700 employees
Market Cap
$45.6 billion
Industry
Net Income
$823.4 million
Founded
1958
5 Year Trend
+12%
Revenue
$4.3 billion
NASDAQ

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