Job details
- Location
- Menlo Park, CA
- Work type
- Onsite
- Compensation
- $100,000 - $150,000/yr
- Posted
- 2 weeks ago
- Apply on
- e2helo.breezy.hr
About this role
E2 - Endovascular Engineering is hiring an Associate Product Manager or Product Manager to support product strategy and lifecycle management for its mechanical thrombectomy platform. The role translates physician needs into product requirements and supports product development, launch, commercialization, and field adoption for VTE treatment technologies.
What you'll do:
- Develop and maintain the product roadmap aligned with clinical, commercial, and corporate priorities
- Collect input on market and user needs through physician interviews, case observation, field feedback, and competitive analysis
- Translate customer insights into clear product requirements, user needs, and design inputs in partnership with R&D
- Monitor the competitive landscape and market dynamics to inform product strategy, pricing, and investment decisions
- Serve as the voice of the customer on cross-functional development teams from concept through launch
- Support design validation, usability studies, and clinical evaluations to confirm the product meets physician and patient needs
- Manage product lifecycle activities, including line extensions, iterative improvements, and SKU and portfolio decisions
- Partner with Quality, Regulatory, and Operations on design controls, labeling, and post-market feedback
- Support/lead launch planning, including segmentation, positioning, messaging, and go-to-market readiness
- Develop product training, technical selling narratives, competitive positioning, and launch toolkits for field sales
- Support case coverage and field partnership to gather real-world feedback and drive successful adoption
- Collaborate with KOLs, advisors, and early adopters to capture procedural insights and validate product direction
What they're looking for:
- 1-5 years of experience
- Experience gathering user needs and translating them into product requirements within a design control environment
- Demonstrated ability to work effectively with engineers and clinicians and to translate between technical and clinical perspectives
- Strong understanding of physician decision-making, procedural workflow, and hospital purchasing dynamics
- Excellent project management, analytical, communication, and cross-functional collaboration skills
- Ability to operate independently with a high degree of ownership and accountability
- Familiarity with FDA design controls, regulatory, and promotional compliance requirements for medical devices
- Bachelor's degree required
- Medical device experience preferred
- Vascular, interventional, or procedural experience preferred
- Experience supporting product development and/or commercial launches in high-growth environments preferred
- MBA or advanced degree a plus
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