Requirements: English
Company: STERIS
Region: Rome , Lazio
Position SummaryThe Senior Quality Inspector is responsible for assisting in the administration of quality functions at a site to ensure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820 / 211, EU MDR, and other applicable regulatory standards. The role supports manufacturing operations of electromedical devices by performing incoming component inspections and in-process controls using advanced measuring instruments. It involves identifying and documenting nonconformances, leading investigations and root cause analyses, and collaborating with engineering teams to troubleshoot and resolve manufacturing issues. The inspector also maintains calibration of monitoring and measuring instruments and interfaces with suppliers for calibration activities.DutiesConduct complex incoming component and in-process product inspections.Initiate and support quality investigations and root cause analyses.Generate incoming inspection plans.Identify and document product and process nonconformances.Identify opportunities for process continuous improvement.Participate in Material Review Board meetings to review nonconformance reports.Support supplier quality improvements through SCARs and site actions.Oversee DHR reviews and batch record release processes.Track trends and report quality data for assigned areas.Perform calibration activities and recordkeeping for inspection equipment.Execute environmental monitoring and maintain records.Complete other duties as assigned.Education and ExperienceAssociates Degree required.Minimum of 3 years of experience in a quality or manufacturing environment or related technical production tasks.Required CompetenciesAbility to work in a fast-paced environment with strict deadlines.Ability to generate detailed, high-quality documentation.Strong analytical and problem-solving skills in technical contexts.Effective teamwork and collaboration skills.Attention to detail and continuous improvement mindset.Proficiency with PC applications, including Excel and Word.Additional InformationWe are committed to equal employment opportunity and affirmative action programs to ensure fair recruitment, hiring, training, transfer, and promotion practices across all job groups, regardless of race, color, religion, age, disability, national origin, citizenship, sex, sexual orientation, gender identity, genetic information, or other protected categories.STERIS is a global leader in healthcare and life sciences products and services, supporting patient care and infection prevention worldwide. We are a publicly traded company with approximately 17,000 associates and serve customers in over 100 countries.Key SkillsQuality inspection, calibration, root cause analysis, continuous improvement, teamwork, documentation, regulatory compliance.Employment DetailsType: Full TimeExperience: 3+ years in relevant fieldVacancy: 1#J-18808-Ljbffr