Job Description
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.
**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.
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