Jobs at Pulse Biosciences, Inc.

General application for future opportunities at Pulse Biosciences, a bioelectric medicine company developing CellFX nsPFA technology for surgical and percutaneous healthcare applications. The company seeks talented individuals to support innovative product development, manufacturing, commercialization, engineering, scientific, clinical, and business activities.

Administer and support corporate IT infrastructure, including Windows servers and PCs, Active Directory, networks, firewalls, VMware, cloud services, backups, and security systems. Troubleshoot helpdesk and infrastructure issues, monitor performance and security, manage incident response, implement technologies, document procedures, coordinate user training, and support infrastructure projects. The role is onsite in Hayward, California, with occasional after-hours and weekend work.

Designs, develops, and maintains automated software testing frameworks for embedded and real-time medical device systems. Develops Python and Shell/Bash test automation, integrates testing with continuous integration workflows, executes functional and risk-based testing, investigates failures, documents defects, and supports FDA-regulated verification and validation. Collaborates with software, systems, electrical, and quality teams, performs code reviews, improves test infrastructure, and mentors engineers.

Supports corporate and securities matters for a Nasdaq-listed medical device company, including SEC and Section 16 filings, insider trading administration, board and stockholder meetings, contracts, legal operations, equity programs, entity management, corporate records, and healthcare compliance. The role also administers legal technology systems, coordinates with transfer agents and outside counsel, and supports employees and executives with equity and legal requirements.

Leads process development and design transfer for catheter devices from early-stage configurations to commercial manufacturing. Responsibilities include DFM/DFA, tolerance analysis, catheter and electrical assembly process optimization, validation, FMEAs, SPC, measurement studies, supplier qualification, sterilization compatibility, lean improvements, ECOs, documentation, and cross-functional collaboration. Mentors junior staff and supports production readiness in a regulated medical-device environment.