Software Design Quality Engineer

Software Design Quality Engineer Job Description Software Design Quality Engineer responsible for developing, maintaining, and managing comprehensive software quality documentation, ensuring their accuracy and regulatory compliance throughout the software lifecycle. Responsibilities: Leads the assessment of software designs by reviewing test and performance data to uphold quality, safety, and regulatory standards, and address engineering deficiencies. Lead in the effective application, compliance, and continuous improvement of policies, procedures, and practices related to software development and validation including software design/verification, risk management, systems validation, traceability and cyber security risk management. Track and risk assess software anomalies for pre‑ and post‑market medical device software. Conduct detailed root cause analyses for software quality issues and validate key design inputs such as usability, reliability, and performance. Assess products and systems to identify defects, abnormalities and design flaws by authoring and executing software test protocols and generating test reports. Implement software quality plans and risk management activities, utilize post‑market analytics to monitor software performance, and initiate corrective actions as needed. Ensure compliance across the product software lifecycle by overseeing regulatory planning and execution for new products and changes as well as managing filings and approvals by overseeing preparation and submission of documentation for global registrations to enable timely market access. Drive regulatory excellence and continuous improvement by developing plans, assessing risks, implementing actions, and optimizing regulatory processes for efficiency while maintaining high compliance standards. Qualifications: Minimum of 5+ years’ experience in FDA regulated, IEC 62304 medical device software environments, with a focus on Software Design Assurance/Control, detailed knowledge of Risk Management (ISO 14971), SDLC and strong understanding of all aspects of the QMS related to Software Design Controls. Proven experience in Root Cause Analysis, Software V&V, identifying/supporting processes and design quality tools for use in tracking/preventing software defects, design traceability, Design for Quality (DfQ), Agile, and SAFe. Strong experience with complex medical systems containing software, hardware and disposables. Ability to share knowledge, insights regarding software quality standards, and regulatory requirements. Excellent written and verbal communication skills, with the ability to communicate and present to all levels of management. Ability to interpret software design and code (C/C++/C# or any other object‑oriented language) to verify implementation of requirements. Minimum of a Bachelor’s Degree (Required) in Quality, Computer Science/Engineering or similar disciplines. ISTQB certification desired. Must be able to successfully perform the following minimum physical, cognitive and environmental job requirements with or without accommodation for this position. Work Location & Requirements: Work is office-based; must be onsite at least 3 days per week with full‑time presence (5 days per week) required. Field roles typically performed outside of company facilities; this position is an onsite role. US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work‑authorized visa, now or in the future. Company relocation benefits will not be provided for this position. You must reside in or within commuting distance to Bedford, MA. May require travel up to 10%. Benefits & Compensation: Pay range in Bedford, MA: $102,480 to $163,968. Actual base pay may vary within the posted range based on factors including experience. Additional compensation such as annual incentive bonus, sales commission or long‑term incentives may be offered. Employees eligible for comprehensive benefits program including generous PTO, 401(k) up to 7% match, HSA with company contribution, stock purchase plan, education reimbursement, and more. Legal Information: Philips is an Equal Employment and Opportunity Employer including Disability/Vets and maintains a drug‑free workplace. #J-18808-Ljbffr Mass Digital Health