Define the multi-year technical roadmap for IVD/LDT software.
Lead feature prioritization for LIMS, lab automation, and sample processing.
Direct integration of diagnostic hardware with cloud/on-prem software.
Ensure software complies with FDA, CLIA/CAP, ISO 13485, and HIPAA/GDPR.
Collaborate with R&D, Molecular Biology, Clinical Lab, Lab Automation, and Eng teams.
Ensure SDLC compliance from concept to launch.

🎯 Requirements

8+ years in Technical Product Management, 4+ in IVD/Medical Devices.
Proven experience with LIMS/LIS and lab automation workflows.
Deep familiarity with FDA software guidelines and CLIA regulations.
BS/MS in Computer Science, Bioengineering, Molecular Biology, or related.
Experience managing and scaling technical product teams in regulated settings.

🎁 Benefits

US base salary range: $220,400 - $281,400.
Equity, bonuses, and comprehensive benefits.
Hybrid work model; Brisbane, CA HQ.
Equal opportunity employer; diverse workforce.

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