Bachelor's degree in Computer Science, Software Engineering, Informatics, Biomedical, or related field; or equivalent experience.
Minimum eight years of software engineering experience in the FDA QSR/ISO 13485 medical device industry.
Proficient in IEC 62304, ISO 14971, IEC 60601, and IEC 62366 standards.
Experience with Agile methodologies like Scrum and Kanban is essential.
Background in web development alongside embedded software development is required.
Familiarity with cloud-based software is preferred.
Responsibilities
Provide expertise in interpreting policies and regulations for compliance assurance.
Collaborate with software development teams on SDLC documentation and reviews.
Engage in Quality Management System activities per FDA and ISO standards.
Participate in software risk management, focusing on cybersecurity.
Stay updated on regulations to ensure compliance of existing software.
Guide development teams in finding solutions to meet regulatory requirements.
Conduct testing to evaluate software effectiveness against performance standards.
Benefits
Comprehensive health insurance options.
Retirement savings plan with company match.
Generous paid time off and holiday schedule.
Opportunities for professional development and training.
Collaborative work environment in a cutting-edge facility.
Full Job Description
Description
Position at Prismatik
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.
About Glidewell
Glidewell is a privately owned dental technology company that provides dental products, services, and education to dental professionals. The company is based in Newport Beach, California and has additional locations in Irvine, California; Louisville, Kentucky; and Dallas, Texas. Glidewell is known for its innovative dental products and services, including BruxZir Solid Zirconia, the most prescribed brand of full-contour zirconia in North America.
