Summary from listing
STERIS is hiring a Quality Analyst to support the administration and continuous improvement of a quality management system in a regulated manufacturing or medical device environment. The role leads complaint and CAPA investigations, supplier and continuous improvement initiatives, nonconformance releases, internal audits, remediation, quality system procedures, statistical analysis, and regulatory compliance activities. It requires a bachelor's degree, 1–5 years of combined manufacturing, quality engineering, or quality systems experience, and experience in an ISO-certified environment; medical device or regulated-industry experience and FDA QSR/EUGMP knowledge are preferred. The position offers $85,000–$95,000, bonus participation, and benefits including healthcare, dental, vision, disability coverage, retirement matching, paid time off, and tuition reimbursement.
