Software V&V Engineer

Location: San Diego CA

Onsite Flexibility: Onsite

• Position Type: Contract
• Contract Duration: 12 months
• Pay Rate: $50.00 / Hour (USD)
• Shift / Schedule: Tuesday through Saturday 2:00 PM 11:00 PM 40 hours per week
• Travel Requirements: None
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

We are currently seeking a System Software Verification and Validation Engineer who will be responsible for testing software for highly complex medical devices/instrumentation for IVD Product Development and IVD Product Testing.

• Design and execute test protocols to verify requirements and design specifications ensuring conformance to intended use of products.
• Conduct system-level tests in the lab to determine product feasibility and support product development.
• Design and conduct reliability lab studies on instruments that run diagnostic assays.
• Candidate must be physically capable and willing to work in a lab environment 67 hours/day performing system-level manual testing on a complex instrumentation platform.

• Strong analytical and problem-solving abilities.
• Attention to detail and ability to follow testing protocols accurately.
• Hands-on aptitude teamwork and strong documentation skills.
• Must be willing and able to work onsite in a laboratory environment.
• Must be willing and able to work the TuesdaySaturday 2:00 PM 11:00 PM shift.
• Must be willing and able to meet all physical requirements of the position.

• Medical device or IVD testing experience.
• Diagnostic assay or instrumentation experience.
• Reliability testing/study experience.
• Test protocol development experience.
• System software testing.
• Experience with regulated verification documentation and requirements traceability.

• Masters or Bachelors degree in Computer Engineering Systems Engineering Biomedical Engineering Bioengineering or a related technical discipline.
• Comparable combination of education and experience may be considered.

• At least one year of system software testing experience.
• We will accept any suitable education training and/or experience combination.

• Laboratory setting.
• Candidates must be able to work in a laboratory setting 67 hours per day.
• Sit; use hands to finger handle or feel objects tools or controls.
• Stand; walk; reach with hands and arms; and stoop kneel crouch or crawl.
• Lifting/moving and carrying products weighing up to 40 pounds.
• Exposure to moving mechanical parts vibration and/or moderate noise levels.
• Exposure to hazardous chemicals or other materials.
• Safety shoes with impact and compression protection must be worn. Closed-toe shoes required.
• Exposure to blood.
• Company badge required for site access.
• Standard onsite parking available.
• Weekend requirement: Yes Saturday is part of the regular schedule.

• Medical Vision and Dental Insurance Plans
• 401k Retirement Fund

This client is a leading medical device manufacturer operating in the IVD (in vitro diagnostics) and womens health space with on-site production and testing facilities. The organization employs engineers manufacturing technicians quality assurance specialists and receiving inspectors who work within an FDA-regulated GMP- and GDP-compliant environment. With a focus on diagnostic and treatment technology teams here include verification and validation engineers quality control professionals and technical documentation specialists collaborating on complex instrumentation platforms.

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking financial services technology life sciences biotech utilities and retail sectors throughout the U.S. and Canada.

Job Number: 26-11705 Industry: Software Engineering

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