Sr. QA Software Engineer (ISO 13485)

Glidewell Laboratories; Irvine (CA); In loco; USD 95.000 - 130.000; Tempo pieno

Descrizione del lavoro

Glidewell Laboratories in Irvine, CA is seeking a senior software engineer to ensure regulatory compliance and lead SDLC activities for medical device software.

This onsite role requires eight years of software engineering experience in FDA QSR/ISO 13485, IEC 62304 and related standards, plus Agile proficiency. Remote work is not available.

Competenze

• Bachelor’s degree in Computer Science, Software Engineering, Informatics, Biomedical, or related technical field; or equivalent experience.
• Minimum eight (8) years of software engineering experience in FDA QSR/ISO 13485 within medical device industry.
• Experience applying IEC 62304, ISO 14971, IEC 60601 and IEC 62366 usability engineering.
• Experience with Agile software development methodologies like Scrum and Kanban.
• Experience with areas beyond embedded software, including web development.

Mansioni

• Provides expertise interpreting regulations to assure compliance.
• Partners with SDLC teams on documentation and design reviews.
• Participates in QMS activities per FDA QSR/ISO 13485.
• Contributes to software risk management and cybersecurity feedback.
• Keeps current on regulations to support software compliance.
• Guides development with regulatory solutions and alternatives.
• Conducts testing and assesses software against standards.

Conoscenze

FDA QSR/ISO 13485 compliance

Software engineering in medical device

IEC 62304 / ISO 14971 / IEC 60601

Agile (Scrum/Kanban)

Web development experience

Formazione

Bachelor’s degree in Computer Science or related field

Strumenti

JIRA/DevOps tools

Descrizione del lavoro

Essential Functions

• Provides expertise and guidance in interpreting policies, regulatory and/or governmental regulations, and internal regulations to assure compliance.
• Partners with software development teams in Software Development Lifecycle (SDLC) documentation including software development plans, software verification and validation, software requirements specifications, software architecture and design documents, design and code reviews, software Risk Management File (RMF), test protocols and reports, traceability matrices.
• Participates in Quality Management System (QMS) activities in compliance with US FDA Quality System Regulations and ISO 13485.
• Participates in software risk management activities including cybersecurity risk by collaborating and providing feedback to software development teams.
• Remains current on existing and new regulations to support compliance of existing software.
• Utilizes knowledge and expertise guide development team in seeking solutions and alternatives to meet regulations.
• Conducts testing and assesses the effectiveness and accuracy of software against existing operating standards or performance guidelines.

Minimum Qualifications

• Bachelor’s degree in Computer Science, Software Engineering, Informatics, Biomedical, or related technical field; or any equivalent education and/or experience from which comparable knowledge, skills and abilities have been demonstrated/achieved.
• Minimum eight (8) years of experience in software engineering in the FDA QSR/ISO 13485 within medical device industry.
• Experience with the application of IEC 62304 (Medical Device Software Lifecycle Processes), ISO 14971 (Risk Management), IEC 60601 (Medical Electric Equipment) and IEC 62366 Usability Engineering, required.
• Experience with Agile software development methodologies like Scrum and Kanban, required.
• Experience with other than embedded software development areas, such as web development, required.
• Previous experience with cloud-based software, preferred.

Pay range: $95,000-130,000k/yr

Leveling and actual compensation may vary based on skills and experience.

This role is fully onsite at our Irvine, CA campus. Remote or hybrid arrangements are not available.