Senior Clinical Engineer, Remote - Bioelectric Medicine

Pulse Staffing Limited; Hayward (CA); Hybrid; USD 100,000 - 140,000; Full time

Benefits offered by this job

Health insurance

401k retirement plan

Stock options

Employee Stock Purchase Plan (ESPP)

Job summary

Pulse Biosciences is seeking a Senior Clinical Specialist, Clinical Engineering to support education and training of physicians and staff on our CellFX devices. The role involves extensive hands‑on work across pre‑clinical, simulated, and clinical settings to ensure safe, effective use.

You will contribute to device deployment, validation, and ongoing collaboration with healthcare providers while advancing regulatory compliance and post‑market activities. Strong travel up to 60% may be required.

Qualifications

• Bachelor’s degree in Biomedical, Electrical, or Mechanical Engineering or related field.
• 6+ years of progressive clinical engineering or medical device experience.
• Experience with Cardiac Ablation Procedures.
• Experience with Class II or Class III devices is highly desirable.
• Strong regulatory knowledge (FDA, ISO 13485) and post‑market surveillance.

Responsibilities

• Provide clinical support for innovative, safe products meeting regulatory standards.
• Support deployment, testing, and validation of devices in clinical environments.
• Offer on-site and remote support during pre-clinical and clinical procedures.
• Train physicians, nurses, and technicians on use and maintenance of devices.
• Collaborate with healthcare providers to optimize device performance.
• Assist with regulatory submissions and ensure complete documentation.
• Mentor other Clinical Specialists within the team.

Skills

Clinical engineering

Regulatory knowledge

Communication skills

Medical devices

Travel readiness

Education

Biomedical/Electrical/Mechanical Engineering degree

Tools

MS Word

Excel

PowerPoint

Job description

Pulse Biosciences is seeking a Senior Clinical Specialist, Clinical Engineering to support education and training of physicians and staff on our CellFX devices. The role involves extensive hands‑on work across pre‑clinical, simulated, and clinical settings to ensure safe, effective use.

You will contribute to device deployment, validation, and ongoing collaboration with healthcare providers while advancing regulatory compliance and post‑market activities. Strong travel up to 60% may be required.