Sr Software Quality Engr - Exempt

Lancesoft; Irvine (CA); On-site; USD 120,000 - 160,000; Full time

Job summary

Lancesoft in Irvine, CA is seeking a Senior Software Quality Engineer to join the Neurovascular Pre-Market Design Quality team. You will work onsite with cross-functional teams to ensure software and system design activities comply with design controls, risk management, and regulatory requirements for medical devices.

The role emphasizes sizing software within the design control lifecycle. The ideal candidate combines systems engineering and software development knowledge with experience in V&V,

Qualifications

• Bachelor's degree in Software/Computer/Electrical/Systems Engineering with 4+ years of experience (or advanced degrees with fewer years).
• Experience with design controls and software lifecycle activities.
• Strong risk management and traceability across requirements, design, and testing.

Responsibilities

• Provide design quality support for software and medical device development.
• Ensure design controls, software lifecycle, and risk management compliance.
• Review system and software requirements, architecture, and design docs.
• Support verification and validation strategies for software and system.
• Collaborate with cross-functional teams to resolve quality issues.
• Perform root cause analysis and oversee corrective actions.
• Mentor junior engineers on design quality and regulatory requirements.
• Contribute to continuous improvement of quality processes.

Skills

Software Quality

Design Controls

Regulatory Compliance

Risk Management

Verification & Validation

Cross-functional Collaboration

Communication

Education

Bachelor's degree in Software/Computer/Electrical/Systems Engineering

Master's degree

PhD

Job description

Job Summary 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

• Provide design quality support for software and software-as a medical device development programs from concept through transfer to manufacturing.
• Ensure compliance with applicable design control, software lifecycle, and risk management requirements.
• Review and contribute to system requirements, software requirements, architecture, and design documentation.
• Support development of verification and validation strategies for software, system, and integration testing.
• Partner with engineering, product development, regulatory, clinical, and quality teams to resolve design quality issues.
• Evaluate software development deliverables for completeness, traceability, and regulatory readiness.
• Support risk management activities, including hazard analysis, software-related risk evaluation, and mitigation verification.
• Participate in design reviews and provide constructive feedback to improve product quality, safety, and compliance.
• Assist in root cause analysis and corrective action activities related to design or software quality issues.
• Mentor less experienced engineers on design quality practices, documentation expectations, and compliance requirements.
• Contribute to continuous improvement initiatives for design quality processes, tools, and templates.

Required Qualifications

• 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.
• Demonstrated experience with design controls, software development lifecycle activities, and verification/validation.
• Strong understanding of risk management principles, design failure analysis concepts, and traceability across requirements, design, and testing.
• Experience supporting cross-functional product development teams.
• Strong written and verbal communication skills with the ability to influence and collaborate effectively.
• Ability to manage multiple priorities in a fast-paced environment.

Preferred Qualifications

• 5 to 8 years of experience in software engineering, systems engineering, design assurance, reliability, or quality engineering in a regulated industry.
• Experience in the medical device industry or another highly regulated environment.
• Knowledge of IEC 62304, ISO 14971, ISO 13485, FDA design control expectations, and related standards.
• Familiarity with agile development environments and how quality practices integrate into iterative development.
• Experience with AI used in process development and embedded in products.
• Experience with software architecture reviews, cybersecurity considerations, or usability/human factors support.
• Advanced degree in engineering or a related discipline.

Core Competencies

• Technical depth in software and systems engineering
• Quality mindset and attention to detail
• Strong analytical and problem-solving skills
• Cross-functional collaboration
• Sound judgment and decision-making
• Effective communication and documentation skills
• Ability to coach and influence without direct authority

Location

This position is based in Irvine, CA, offering a vibrant environment with a blend of natural beauty, cultural attractions, and a thriving tech industry. Working on-site full-time, you'll be part of a dynamic team committed to delivering high-quality medical device solutions.