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Pharmavise Corporation seeks a Software Development Verification Engineer III for its Medical Device division, hybrid setup in Valencia, CA. You will join Neuromodulation Software Development, focusing on test automation, connectivity projects, and robust software verification to improve patient outcomes.
The role requires collaborating with cross-functional teams, mentoring junior SDET engineers, and performing requirements analysis, verification, and automation across desktop, mobile, and
Valencia, United States | Posted on 11/12/2026
From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com and follow us on LinkedIn: https://www.linkedin.com/company/pharmavisecorp
Our Medical Device client has an exciting opportunity for a Software Development Verification Engr III.
Job Summary:
Client is seeking a highly motivated and versatile Sr. Software Development Engineer in Test to join Neuromodulation Software Development team of diverse and high-performing employees, tackling some of the most important health industry challenges. As an engineer on the Software Infrastructure, Framework and Tools team, you will be collaborating on various exciting projects, ranging from test automation to connectivity projects.
In this pivotal role, you will be expected to leverage your extensive experience to tackle complex technical challenges and drive innovation within the team. Your proactive approach and problem-solving skills will be crucial as you navigate the intricacies of software testing and development. By embracing new technologies and methodologies, you will ensure the robustness and reliability of our software solutions, thereby contributing to our mission of improving patient outcomes through cutting-edge neuromodulation technologies. Your collaboration with cross-functional teams will be instrumental in achieving our strategic goals and delivering high-quality products to the market.
This individual will partner with product development, participate in architectural and software development activities, mentor junior SDET engineers, and conduct software requirements analysis, verification, test documentation and automation.
Responsibilities and Job Requirements:
Other Details:
Schedule: 40 hours
Work Set-Up: Hybrid (3 days onsite) with option to work at 1 of these sites:
Start Date: 12/7/2026
Required Qualifications:
Preferred Qualifications:
Pharmavise Corporation is an Equal Opportunity Employer and does not discriminate on the basis of race or ethnicity, religion, sex, national origin, age, veteran disability or genetic information or any other reason prohibited by law in employment.