We use cookies. Find out more about it here. By continuing to browse this site you are agreeing to our use of cookies.
#alert
Back to search results
New

Software Quality Engineer

Spectraforce Technologies
United States, California, Alameda
Jul 20, 2026
Role: Software Quality Engineer

Duration: 1 year (Possibility of extension or conversion)

Location: Alameda CA (Onsite)

Job Description:

* Participates as a member of the Software Quality Assurance (SWQA) team for Diabetes Care products that ensures digital applications produced by ADC is developed, validated, and maintained in compliance with regulatory, corporate and divisionalrequirements.

* Review quality system documentation products as they apply to the development,verification, validation, use, and maintenance of medical device software.

* Coordinate activities with other engineering disciplines, departments, and contractors.

Duties:

* Completes software quality tasks in accordance with current Quality System Requirements.

* Works independently with objectives given by SWQA Manager.

* Can plan and coordinate own work according to higher-level project schedules.

* Reviews deliverables/activities as identified in the ADC Design Control Process/project plan or equivalent project plan. * Including System Specifications/Requirements documents,Verification Test Cases, Verification/Validation protocols, Trace Matrices andVerification/Validation Summary Reports for the Alameda site.

* Ensures unexpected events, issues or software bugs which occur during verification/validation are addressed and/or processed under relevant design control and defect management procedures.

* Ensures compliance to relevant FDA QSR, ISO guidelines (ISO 13485, ISO 14971), including 21 CFR Part 11 and Diabetes Care requirements as they relate to the development, verification, validation, and maintenance of medical device software.

Qualifications:

* Bachelor's degree, or equivalent experience, in a scientific, technical, or engineering discipline.

* 2 to 5 years' experience in Software Quality Assurance and/or Software Testing experience.

* Knowledge of FDA QSR, relevant ISO guidelines and 21 CFR Part 11. Has knowledge of Design Control requirements.

* Must have 1 - 3 years project experience in software quality assurance practices, methodologies including Agile and techniques, preferably in medical device software such as web and mobile applications.

* Must have excellent oral and written communication skills.

* ASQ Certifications a plus.

* Medical Device experience strongly preferred.

* Cybersecurity, medical web and mobile applications or AI experience preferred.
Applied = 0

(web-77cf7d65c7-rcc7h)