Select how often (in days) to receive an alert:At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.Position SummaryThe Senior Quality Inspector is responsible for assisting in the administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Senior Quality Inspector supports the manufacturing operations of electromedical devices by performing incoming component inspections and in-process controls of products using advanced measuring instruments. Identifies and documents component, process, and product non-conformances and leads investigation/root-cause countermeasure activities. Collaborates with the manufacturing engineering team in troubleshooting investigations and manufacturing process problem-solving. Is responsible for maintaining the calibration status of monitoring and measuring instrumentation in the quality inspection and production department, interfacing directly with suppliers for calibration.DutiesConducts complex incoming component and in-process product inspections.Initiates and supports quality investigations and associated problem-solving/root-cause activities.Generates incoming inspection plans.Identifies and documents product and process non-conformances.Identifies opportunities for process continuous improvement.Participates on a Material Review Board to review and process non-conformance reports.Supports supplier quality improvements through SCARs and other site actions.Oversees DHR reviews and batch record release.Tracks, trends, and reports quality data for assigned areas.Performs site calibration activities and recordkeeping for inspection equipment.Executes environmental monitoring processes and recordkeeping.Completes other duties as assigned.Education DegreeAssociate's DegreeRequired Experience and Competencies1-3 years of experience required in a quality/manufacturing environment or other technical production tasks.Ability to work in a fast-paced environment with strict deadlines.Ability to generate detailed, high-quality documentation.Ability to work with others in analyzing and solving technical problems.Teamwork: Collaborates with others. Works in a professional manner to support team actions.Effectively manages work tasks. Is detail-oriented and strives for continuous improvement.PC experience and working familiarity of common desktop applications including Excel and Word.Additional InformationWe are committed to equal employment opportunity and the use of affirmative action programs to ensure that persons are recruited, hired, trained, transferred, and promoted in all job groups regardless of race, color, religion, age, disability, national origin, citizenship status, sex, sexual orientation, gender identity, genetic information, and any other category protected by state or local law.STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. WE HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD by providing innovative healthcare, life sciences, and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and customers in more than 100 countries.STERIS strives to be an Equal Opportunity Employer.Job Segment: Inspection, Inspector, Quality Control Inspector, Infection Control, Manufacturing Engineer, Engineering, Quality, Healthcare
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