End-to-End Medical Device Program Manager

Element Science

United States

On-site

USD 140,000 - 160,000

Full time

5 days ago
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Benefits offered by this job

Stock options
Health insurance (90% employer‑paid)
401(k) retirement plan
Paid time off
Paid holidays
FSA
HSA
Employee assistance program

Job summary

Element Science is seeking an experienced Technical Project Manager to lead cross‑functional projects spanning the full medical device product lifecycle, from early‑stage research and development through design, verification and validation, manufacturing, commercialization, and into the hands of patients who depend on our life‑saving technology.

The ideal candidate brings hands‑on experience guiding medical devices from concept through commercialization, a strong understanding of regulatory

Qualifications

  • Bachelor’s degree in Electrical, Mechanical, Biomedical, Systems Engineering, or related field.
  • 5+ years in medical device industry with full lifecycle PM experience.
  • Experience leading devices through full lifecycle from concept to post‑market.

Responsibilities

  • Lead cross‑functional projects across R&D, design verification, manufacturing, and commercialization.
  • Align requirements, quality, and regulatory expectations across teams.
  • Drive readiness for design reviews, verification/validation, and manufacturing.
  • Support product improvements from field experience and patient needs.

Skills

Project management
Cross-functional leadership
Regulatory understanding
Technical translation
Stakeholder coordination

Education

Bachelor's degree in Electrical, Mechanical, Biomedical, Systems Engineering

Job description

Element Science is seeking an experienced Technical Project Manager to lead cross‑functional projects spanning the full medical device product lifecycle, from early‑stage research and development through design, verification and validation, manufacturing, commercialization, and into the hands of patients who depend on our life‑saving technology.

The ideal candidate brings hands‑on experience guiding medical devices from concept through commercialization, a strong understanding of regulatory

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