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 Summary**:The Quality Engineering Supervisor leads a team of quality engineers, technicians and inspectors focused on process and product quality improvement for multiple production lines/values streams.
This role has responsibility for incoming product/component inspection, NCR investigation, production quality and final QC inspection/testing.
The Quality Engineering Supervisor has responsibility for internal and customer facing key metric performance for assigned production lines/value streams.
**Duties**:- Lead assigned Quality team focused on overall manufacturing/servicing quality improvement for key internal and customer facing metrics.
(OOB, SR/Unit, Installation DPU, others)- Lead assigned Quality team focused on internal production quality by improving component and process non conformances; production line DPU (defect per unit); production FPY (first pass yield).- Lead assigned Quality team to improve customer facing and internal product/service and process quality key metrics through robust data analysis and improvement/problem solving projects.- Prepare & present quality data on assigned processes/areas at Management Review- Lead project related with the key QS initiatives defined by Corporate.- Meet the regulations and special requirements from the certified bodies and customers.- Production and Pos-Production analysis for site products- New Product Introduction support to assure compliance with QMS and International regulations applicable.- Lead assigned Quality staff in effectively managing nonconforming product including proper disposition and recordkeeping.- Supports process validation activities with the engineering teams.
**Education Degree**:- Bachelor's Degree in Mechanical Engineering or Other**Required Experience**:- 5-8 years of Quality Engineering experience.- 5-8 years of experience in healthcare, medical device or other regulated industry preferred.- 5-8 years of experience working within a regulated or certified Quality Management System required.- 3-5 years of experience with supplier quality.- 3-5 years of experience in Lean methods.- ASQ, QSR, or familiarity with QSR/GMP regulations preferred.- 3-5 supervising/leading employees.- Bilingual- Bachelor's Degree Mechanical, Industrial, or related.- Lean Manufacturing Certification or related preferred.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.