Senior Systems Verification Engineer – Medical Devices

Wipro Technologies; Pleasanton (CA); On-site; USD 80,000 - 160,000; Full time

Benefits offered by this job

Medical and dental benefits

Disability insurance

Paid time off

Job summary

Wipro Limited in Pleasanton, California, is seeking a seasoned verification professional to lead system-level verification for complex hardware–software products. You will drive verification planning, test development, and services for regulated environments.

The role requires strong requirements engineering, risk management, and cross-functional collaboration, with a focus on delivering robust verification for medical device programs.

Qualifications

• Bachelor's degree in a technical field with 5–6 years of relevant experience.
• Master's degree in a related technical field with at least 4 years of relevant experience.
• Experience leading system-level verification for complex hardware–software products.
• Experience in regulated product development environments (medical devices preferred).
• Strong knowledge of requirements engineering, traceability, and verification methodologies.
• Experience in risk management and verification of risk controls.

Responsibilities

• Lead verification efforts for complex hardware–software products.
• Develop verification plans, protocols, test methods, and verification reports.
• Communicate complex technical information clearly to diverse stakeholders.
• Independently drive verification activities in cross-functional environments.
• Support regulatory submissions for Class II and/or Class III medical devices.

Skills

VLSI-Verification Planning

Education

Bachelor's or Master's in a related technical field

Master's degree in related technical field

Job description

Wipro Limited in Pleasanton, California, is seeking a seasoned verification professional to lead system-level verification for complex hardware–software products. You will drive verification planning, test development, and services for regulated environments.

The role requires strong requirements engineering, risk management, and cross-functional collaboration, with a focus on delivering robust verification for medical device programs.