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The Quality Analytics Analyst is responsible for assisting in administration of the quality analytics function to support the STERIS AST Quality and Operations analysis function globally. This position assists with the development and implementation of quality and operational analysis and reporting in various systems to support management review and decision-making. This position is active in supporting performance improvement initiatives and provides inputs for analysis that is presented to senior management and local site management across all AST facilities. The individual is responsible for completing assigned reporting and analytic requirements provided by internal and external Customers.
Job Responsibility:
Coordinate individual day-to-day tasks to complete recurring (Monthly/Quarterly/Annually) reporting requirements for Quality Analytics function
Execute data refreshes and reporting updates at regular intervals
Provide reporting and analytics for non-conformance trending
Initiate and/or participate in corrective actions, problem-solving and continuous improvement activities
Travel to AST facilities, domestically and/or globally, to support remediation activities, audits/inspections and/or continuous improvement initiatives
Perform internal reviews of data trends among multiple systems, create reporting to illustrate data trending issues, and develop and execute actions to remediate any negative data trends
Create or amend process documentation for reporting within the Quality Analytics function
Review collected data to perform statistical analysis and recommend process changes to improve quality
Monitor and report on performance metrics
Instruct other STERIS employees in quality principles, effective corrective actions, and valid statistical techniques
Collaborate with other departments and facilities within the company on quality related issues
Support development of reports to enhance the STERIS quality system programs
Ensure the accuracy of reporting data and analytics to meet external and internal requirements according to documented policies, procedures, standards and regulations
Perform other duties as assigned
Requirements:
Bachelor's Degree
1-5 years of combined statistical analysis and/or data management and analytics experience
1-5 years of experience with medical device or other regulated industries preferred
1-5 years of experience working in an ISO certified environment required
Working knowledge of FDA QSR/ EUGMP regulations strongly preferred
Advanced knowledge of data analytics tools such as SQL, Tableau, Minitab, etc. is preferred
Nice to have:
Experience with medical device or other regulated industries
Advanced knowledge of data analytics tools such as SQL, Tableau, Minitab