Software Quality Engineer
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Days Left: 26 days, 4 hours left Apply Engineer, Software Quality Location: Pleasanton, CA, 55442 Work Arrangement: 100% Onsite Duration: Contract - 12 Months Potential: Possibility of conversion to permanent Business Unit: Heart Failure Hours: Monday-Friday, 8:00 AM-5:00 PM Position Overview We are seeking an Engineer, Software Quality to support software quality, compliance, verification and validation, risk management, and continuous improvement activities within a regulated medical device environment. This role will work closely with Software Engineering, Systems Engineering, Quality, Regulatory, Cybersecurity, and other cross-functional teams to ensure software and system development activities meet applicable quality and regulatory requirements. The ideal candidate will have a strong quality and process-oriented background with an understanding of software development and validation, rather than a heavy software testing or test automation background. Key Responsibilities
- Support software verification and validation (V&V) activities, including development and review of test protocols, plans, reports, and related quality documentation.
- Support assessments of non-product software and associated quality requirements.
- Support product cybersecurity assessments in collaboration with cross-functional teams.
- Review software and system documentation to ensure quality, consistency, and regulatory compliance.
- Maintain requirements traceability and support software development lifecycle (SDLC) processes.
- Perform and support risk assessments, including FMEA and hazard analysis.
- Identify quality issues, facilitate root-cause analysis, and support timely issue resolution.
- Participate in sustaining engineering activities, including post-release support and issue resolution.
- Participate in design reviews and represent Quality during applicable review and approval activities.
- Support post-release software changes and ensure appropriate quality and compliance processes are followed.
- Support internal and external audits, including audit readiness and response activities.
- Identify and support quality system and process improvements.
- Collaborate with cross-functional teams to ensure compliance with applicable FDA and industry requirements.
- Contribute to continuous improvement of software quality processes, documentation, and controls.
- Bachelor's degree in Computer Science, Software Engineering, Systems Engineering, or a related technical field.
- Minimum 2 years of experience in software quality, software validation, systems engineering, quality engineering, or a related discipline.
- Experience working within a regulated industry, preferably medical devices, diagnostics, pharmaceutical, or another highly regulated environment.
- Understanding of software quality and software verification and validation processes.
- Experience with requirements traceability and software development lifecycle processes.
- Knowledge of risk management, including FMEA and/or hazard analysis.
- Strong understanding of quality and compliance principles.
- Strong analytical, problem-solving, written, and verbal communication skills.
- Ability to work independently with minimal supervision while collaborating effectively with cross-functional teams.
- Experience in a medical device environment.
- Knowledge of FDA regulations and quality requirements.
- Experience with ISO 13485.
- Experience with IEC 62304.
- Experience supporting quality or regulatory audits.
- Experience with CAPA, nonconformance, deviation, or issue-resolution processes.
- Experience with process improvement and quality system improvement initiatives.
- Familiarity with software cybersecurity quality requirements.
- Quality Engineer
- validation
- verification
- plans
- reports
- FMEA
- SDLC
- Recruiter
- Phone
- Osama Patel Nur Mohammed
- View email address on click.appcast.io
Vacancy posted 5 days ago
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