
Senior Quality Systems Engineer
- Durham, NC
- $91,000-114,000 per year
- Permanent
- Full-time
- Support Quality through interpretation, establishment, and execution of quality engineering concepts and principles, in accordance with GRAIL's quality management system and regulatory requirements, including ISO 13485, ISO 14971, 21 CFR 820, IVDR, CAP/CLIA/NYSDOH, ISO 15189, and related regulations and standards.
- Use proactive, creative problem-solving to contribute to the development of concepts and principles to achieve goals and objectives.
- Demonstrate technical proficiency, creativity, teamwork, collaboration, and independent thought.
- Exercise good judgment within broadly defined practices and policies when selecting methods, techniques, and evaluation criteria for results.
- Act independently with regular oversight to determine methods and procedures to successfully complete assignments.
- Structure day-to-day work autonomously, effectively communicating status and issues to management.
- Identify and evaluate deficiencies and improvement opportunities, working cross-functionally to resolve and improve existing processes.
- Demonstrate increasing technical proficiency by solving progressively complex problems and operating with greater independence.
- Implement and manage GRAIL's Standards Watch program (e.g., BSI Compliance Navigator, CLSI, ANSI), including the analysis, administration, and maintenance of internal standards libraries. This includes managing user accounts and access in Compliance Navigator and related systems, as well as ensuring timely updates to reflect evolving industry standards.
- Conduct internal audits to ensure ongoing compliance with ISO 13485, ISO 14971, 21 CFR 820, IVDR, CAP/CLIA/NYSDOH, ISO 15189, and other applicable standards and regulations. Actively manage audit findings to completion.
- Perform various gap assessments, including CAP/CLIA checklists, to ensure adherence to clinical laboratory requirements and ongoing accreditation needs.
- Manage the quality planning process, including tracking status, reviewing progress of individual owners, and reporting on key metrics.
- Oversee the maintenance and renewal of licenses and certificates, including ISO certifications and clinical laboratory licenses, ensuring all licenses and certifications are current and in good standing.
- Compile Quality System trend data and prepare presentations for Quality Management Review meetings.
- Support education and training initiatives to strengthen the inspection readiness program throughout GRAIL.
- Perform other duties as assigned.
- Bachelor's degree in science, engineering, or other technical area.
- Master's degree in a related technical area, or MBA preferred
- Minimum of 5 years (corresponding to level) of experience working within a clinical laboratory (high complexity CLIA/CAP environment) or related (e.g., IVD medical device, pharma, etc.) quality management system.
- Experience working with applicable regulations and standards including CAP/CLIA, New York State Department of Health, ISO 13485, ISO 15189, and other applicable industry requirements.
- Experience supporting regulatory inspections/audits and responding to findings.
- Excellent written and verbal communication skills.
- Ability to comprehend and interpret technical information.
- Next Generation Sequencing (NGS) experience preferred
- ASQ Certified Quality Auditor, Certified Quality Engineer, or similar.