Medical Device Software Engineering Manager

Vero Biotech

Atlanta (GA)

On-site

USD 140,000 - 180,000

Full time

14 days+
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Job summary

Vero Biotech seeks an experienced Manager, Software Engineering (R&D) to lead software and firmware development for the GENOSYL DS platform. This working manager role requires deep technical credibility in architecture reviews, code reviews, and defect triage, while guiding the team and driving the roadmap with clear milestones.

The ideal candidate translates user and clinical needs into software requirements, collaborating with clinical, Quality/Regulatory, systems, hardware R&D, and

Qualifications

  • Eight or more years of software development experience in medical devices including embedded software/firmware.
  • Experience leading engineers through real product delivery and managing timelines.
  • Strong knowledge of FDA software guidance, design controls, and regulatory submissions.

Responsibilities

  • Lead day-to-day software and firmware development efforts for the GENOSYL DS platform.
  • Own software architecture, interfaces, and risk-based design controls across multiple generations.
  • Translate user/clinical needs into software requirements and drive cross-functional collaboration with clinical, Quality/Regulatory, hardware R&D, and manufacturing teams.
  • Manage roadmap, milestones, risks, and releases to ensure on-time delivery of objectives.

Skills

Software leadership
Embedded software
End-to-end development
Regulatory knowledge
Architecture reviews
Cross-functional collaboration

Education

Bachelor's or Master's in CS/EE/SE

Job description

Vero Biotech seeks an experienced Manager, Software Engineering (R&D) to lead software and firmware development for the GENOSYL DS platform. This working manager role requires deep technical credibility in architecture reviews, code reviews, and defect triage, while guiding the team and driving the roadmap with clear milestones.

The ideal candidate translates user and clinical needs into software requirements, collaborating with clinical, Quality/Regulatory, systems, hardware R&D, and

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