Software Validation Engineer
Primary Talent Partners· Staffing And Recruiting· Sep 30, 2026 · 27d ago
Irvine, CA
In office
Contract · 7 months
Mid
$64–$67/hr
4+ years exp
Job description
Primary Talent Partners has a new contract opening for a Sr Software Quality Engr with our medical device client in Irvine, CA. This is a 7-month contract with a potential for extension.
Pay: $64.00 - $67.00/hr ; W2 contract, no PTO, no Benefits. ACA-compliant supplemental package available for enrollment. Candidates must be legally authorized to work in the United States and must be able to sit on Primary Talent Partners W2 without sponsorship.
Description:
The Senior Software Quality Engineer on the Neurovascular Pre-Market Design Quality team will partner with cross-functional development teams to ensure software and system-level design activities are planned, executed, and documented in compliance with applicable quality and regulatory requirements. This role supports new product development by providing quality oversight and technical guidance throughout the design control lifecycle, with a focus on neurovascular device sizing software as a medical device system.
The ideal candidate combines strong systems engineering and software development knowledge with experience in design controls, risk management, verification and validation, and regulatory expectations for medical device development.
Key Responsibilities
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Provide design quality support for software and software-as a medical device development programs from concept through transfer to manufacturing.
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Ensure compliance with applicable design control, software lifecycle, and risk management requirements.
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Review and contribute to system requirements, software requirements, architecture, and design documentation.
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Support development of verification and validation strategies for software, system, and integration testing.
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Partner with engineering, product development, regulatory, clinical, and quality teams to resolve design quality issues.
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Evaluate software development deliverables for completeness, traceability, and regulatory readiness.
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Support risk management activities, including hazard analysis, software-related risk evaluation, and mitigation verification.
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Participate in design reviews and provide constructive feedback to improve product quality, safety, and compliance.
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Assist in root cause analysis and corrective action activities related to design or software quality issues.
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Mentor less experienced engineers on design quality practices, documentation expectations, and compliance requirements.
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Contribute to continuous improvement initiatives for design quality processes, tools, and templates.
Required Qualifications:
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Bachelor's degree in Software Engineering, Computer Engineering, Electrical Engineering, Systems Engineering, or a related technical field and minimum of 4 years of relevant experience OR Master's degree with a minimum of 2 years relevant experience OR PhD with 0 years relevant experience.
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Demonstrated experience with design controls, software development lifecycle activities, and verification/validation.
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Strong understanding of risk management principles, design failure analysis concepts, and traceability across requirements, design, and testing.
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Experience supporting cross-functional product development teams.
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Strong written and verbal communication skills with the ability to influence and collaborate effectively.
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Ability to manage multiple priorities in a fast-paced environment.
Preferred Qualifications:
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5 to 8+ years of experience in software engineering, systems engineering, design assurance, reliability, or quality engineering in a regulated industry.
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Experience in the medical device industry or another highly regulated environment.
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Knowledge of IEC 62304, ISO 14971, ISO 13485, FDA design control expectations, and related standards.
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Familiarity with agile development environments and how quality practices integrate into iterative development.
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Experience with AI used in process development and embedded in products.
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Experience with software architecture reviews, cybersecurity considerations, or usability/human factors support.
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Advanced degree in engineering or a related discipline.
Core Competencies:
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Technical depth in software and systems engineering
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Quality mindset and attention to detail
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Strong analytical and problem-solving skills
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Cross-functional collaboration
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Sound judgment and decision-making
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Effective communication and documentation skills
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Ability to coach and influence without direct authority
This position plays a critical role in delivering safe, effective, compliant, and high-quality products for our patients and customers by ensuring software and system design activities meet high standards for quality throughout the development lifecycle.
TECHNICAL SKILLS
Must Have
• Computer and software validation
• Change control of Medical Devices
• Conducted software risk analysis
• Control software verification
• Develop Software Risk Analysis
• Software risk analysis
Top Needs:
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Software coding experience (C, Java, Python etc..)
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Software Risk Assessment
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Software Verification and Validation
Education Required: Bachelor's or Masters in Engineering degree
Years' Experience Required: 5 + years
Primary Talent Partners is an Equal Opportunity / Affirmative Action employer committed to diversity in the workplace. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, age, national origin, disability, protected veteran status, gender identity, or any other factor protected by applicable federal, state, or local laws.
If you are a person with a disability needing assistance with the application or at any point in the hiring process, please contact us at info@primarytalentpartners.com
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