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    Sr. Quality Assurance Engineer - Irvine, United States - Glidewell

    Glidewell
    Glidewell Irvine, United States

    5 days ago

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    Description

    Description

    Position at Prismatik

    Essential Functions :

  • Leads the ongoing implementation of Software Quality Management System (QMS) in conformance with US FDA Quality System Regulations and ISO 13485 Design Controls, through the integration of internal and external/medical device industry best practices.
  • Responsible for the administration of the QMS software.
  • Collaborates with software development teams in the creation of Design History Files (DHFs) including software development plans, software verification and validation plans, software requirements specifications, software architecture and design documents, design and code reviews, software Risk Management File (RMF), test protocols and reports, traceability matrices.
  • Conducts investigations and provides corrective and preventive actions based on analysis and review. Provides and implements effective solutions that will drive continuous and measurable improvements.
  • Integrates ISO 14971, risk management and IEC 62366 usability engineering activities with Glidewell/Prismatik processes.
  • Mentors and provides direction to software development teams in design controls and lead risk management activities.
  • Fosters and maintains organizational compliance to the quality system including ongoing training and education on software QMS and Prismatik framework.
  • Provides CAPA, complaints, audit and overall QMS support in regards to software.
  • Performs other related duties and projects as business needs require at direction of management.

    • Education and Experience:

  • Bachelor's degree in Computer Science, Software Engineering, Informatics, Biomedical, or related technical field or equivalent practical experience.
  • Minimum of eight (8) years of experience in software design assurance in the FDA QSR/ISO 13485 medical device industry.
  • Experience with the application of IEC Medical Device Software Lifecycle Processes), ISO Risk management) and IEC 62366 Usability Engineering.
  • Experience with Agile software development methodologies like Scrum and Kanban.
  • Experience with other than embedded software development areas, such as web development.
  • Previous experience with digital health, Health IT or mobile medical applications required.
  • Previous experience with cloud-based software preferred.
  • Knowledge of CAD/CAM and AI/ML a plus.

    • Knowledge, Skills, and Abilities:

  • Advance knowledge with development and test requirements with recognized standards (ISO
  • Demonstrated knowledge of the application of regulatory requirements for wellness, low-risk and high-risk software applications using a scalable approach to the Prismatik practices and the QMS.
  • Demonstrated knowledge and understanding of software development, including cloud computing.
  • Demonstrated ability to implement and improve Software QMS processes.
  • Demonstrate knowledge of group software development methods (Agile Process and Scrum Method).
  • Advance knowledge on writing, executing and monitoring automated test suites using a variety of technologies (Selenium, WebDriver, JavaScript and Nodejs).
  • Demonstrated knowledge of AWS architecture and tools (EC2, Lambda, RDS, Dynamo DB, RedShift, SQS, S3, API Gateway, Kinesis, and CloudWatch).
  • Demonstrated time-management skills to complete assignments while meeting critical deadlines.
  • Ability to contribute effectively as a member of a team and work cohesively as a part of a team.
  • Possess a strong attention to detail and accuracy.
  • Proficient knowledge of general office procedures and office machines.
  • Ability to effectively prioritize duties and efficiently complete responsibilities.
  • Ability to work beyond normal business hours to meet critical deadlines and resolve emergency issues.
  • Ability to travel within company premises occasionally, both domestically and internationally, depending on project requirements.
    • Pay:$110K-$135K

    Glidewell Laboratories is the industry leader in dental technology due to our agility, speed, and cutting edge technology. We work in a fast-paced and highly sought-after employee-friendly work environment. Behind all of this success is an amazing group of people who are passionate about bringing innovation to the marketplace, while providing quality and affordability to better the lives of people all over the world. If you share in our passion for teamwork and a vision for excellence, let's talk about a rewarding career at Glidewell

    In addition are the following generous employee benefits: Medical, Dental, Vision, 401K with company match, company-paid life insurance, additional onsite dental services, vacation, holiday, and sick time, employee gym (with fitness classes and meditation room), employee medical/wellness center (with massage therapy and acupuncture), two company subsidized cafes, Internet cafes, employee lounges with big screen TVs, game tables, fun company sponsored events, a diverse work environment with over forty nationalities represented, and much more

    Glidewell Laboratories is an Equal Opportunity Employer and prohibits any kind of unlawful discrimination and harassment. We are committed to the principle of equal employment opportunity for all employees and to provide employees with a work environment free of discrimination and harassment on the basis of race, color, religion, national origin, sex, age, physical or mental disability, veteran status, sexual orientation, gender identity, genetic information, or any other status protected by the statutes, rules, and regulations in the locations where it operates. If you are an individual with a disability and need a reasonable accommodation to assist with your job search or application for employment, please contact us at Please indicate the specifics of the assistance needed.

    Note to Current employees: Please apply through Employee Transfer Application to complete the transfer request form.

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