Join Steris as Supervisor, Quality Control in PLYMOUTH Minnesota. At the Steris you will perform tasks as listed below, Apply Steris Quality careers in PLYMOUTH MN.
Position : Supervisor, Quality Control
Job Category: Quality
Work location : PLYMOUTH, Minnesota
Job Segment : QC, Medical Device, Inspector, Manager, Quality Manager, Quality, Healthcare, Management
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.
The Quality Control Supervisor leads a team of Quality Technicians or Inspectors focused on incoming or final product/component inspection. The Quality Control Supervisor develops and manages technician/inspector work assignments and ensure products or components.
In addition, as a contributor to Quality System compliance, the Quality Supervisor supports the site to ensure the Quality System adheres to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other regulatory standards, as applicable.
What You Will Do:
Lead and supervise assigned Quality staff to effectively execute QC final product inspection procedures and capture associated non-conformances.
Lead and supervise assigned Quality staff to effectively execute QC component inspection procedures and capture associated non-conformances.
Lead and supervise assigned Quality staff in effectively documenting and investigating QC non-conformances.
Lead and Supervise assigned Quality staff in effectively managing nonconforming devices and materials including proper disposition and recordkeeping.
Provide Quality data analysis and trending support to drive product/service and process improvements.
Manage assigned Quality staff work schedules and assignments.
Lead QC function planning as an input to the overall site Quality Objective plan.
Lead the team’s talent development processes and knowledge development.
What You Will Need To Be Successful:
6+ years of production Quality and/or Quality Management Systems experience.
3-5 years of experience in healthcare, medical device or other regulated industry.
3-5 years of experience in a team lead role and/or supervising employees.
ASQ, QSR, or familiarity with QSR/GMP regulations preferred.
STERIS is a leading provider of products and services that meet the needs of growth areas within Healthcare: procedures, devices, vaccines and biologics. We exist to fulfill our MISSION TO HELP OUR CUSTOMERS CREATE A HEALTHIER AND SAFER WORLD. STERIS is a $3B, publicly traded (NYSE: STE) company with approximately 16,000 associates and Customers in more than 100 countries.
If you need assistance completing the application process, please call 1 (440) 392.7047. This contact information is for accommodation inquiries only and cannot be used to check application status.
STERIS is an Equal Opportunity Employer. We 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, military or veteran status, sex (including pregnancy, childbirth and related medical conditions), sexual orientation, gender identity, genetic information, and any other category protected by federal, state or local law. We are not only committed to this policy by our status as a federal government contractor, but also we are strongly bound by the principle of equal employment opportunity.
The full affirmative action program, absent the data metrics required by § 60-741.44(k), shall be available to all employees and applicants for employment for inspection upon request. The program may be obtained at your location’s HR Office during normal business hours.
Nearest Major Market: Minneapolis
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