Quality Control Supervisor

<div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>Position Summary</b></H2></div><div><p>The Quality Control Supervisor in our Plymouth, MN location 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 are in specification and are compliant with applicable regulations/requirements. </p><p>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.</p><p> </p><p><strong>This position requires working onsite in our Plymouth, Minnesota location 7:00am to 4:00pm Monday through Friday. </strong></p></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>What You'll do as a Quality Control Supervisor </b></H2></div><div><p><strong> </strong></p><ul><li>Lead and supervise assigned Quality staff to effectively execute QC final product and component inspection procedures and capture associated non-conformances.</li><li>Lead and supervise assigned Quality staff in effectively documenting and investigating QC non-conformances and effectively managing nonconforming devices and materials including proper disposition and recordkeeping.</li><li>Provide Quality data analysis and trending support to drive product/service and process improvements.</li><li>Manage assigned Quality staff work schedules and assignments.</li><li>Lead QC function planning as an input to the overall site Quality Objective plan.</li><li>Lead the team’s talent development processes and knowledge development.</li><li>Perform other duties as assigned</li></ul></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>The Experience, Skills and Abilities Needed </b></H2></div><div><p><strong>Required: </strong></p><ul><li>Vocational / Technical degree or Associates Degree in an Engineering or Scientific related field.</li><li>Minimum of 6 years of production Quality and/or Quality Management Systems experience.</li><li>Minimum of 3 years of experience in healthcare, medical device or other regulated industry.</li><li>Minimum of 3 years of experience in a team lead role and/or supervising employees.</li></ul><p><strong> </strong></p><p><strong>Preferred: </strong></p><ul><li>ASQ, QSR, or familiarity with QSR/GMP regulations preferred</li><li>Experience collaborating across functions.</li><li>Proficiency working with Windchill PLM, SAP, Oracle, and/or TrackWise. </li><li>Ability to lead Kaizen events and participate in CAPA events.</li><li>Strong people leader skills including ability to effectively develop a team.</li></ul><p> </p><p><strong> </strong></p><p><strong>Other: </strong></p><ul><li><strong> </strong>Customer Focused: Demonstrates a “Customer first” mindset.

Responds with a sense of urgency.</li><li>Teamwork: Collaborates with others. Works in a professional manner to support team actions. </li><li>Results: Effectively manages work tasks.

Is detail oriented and strives for continuous improvement. Ability to analyze technical issues.

Ability to cope with change and shifting priorities.</li><li>Communication: Constructs clear written communication. Keeps manager and co-workers informed.</li><li>Job Knowledge: PC experience and working familiarity of common desktop applications including Excel and Word.</li><li>Initiative/Leadership: Takes ownership of task and projects and seeks clarification if unsure of direction.</li><li>Ability to analyze and interpret data; utilize problem solving methodologies and drive process improvements</li></ul><p><strong> </strong></p></div></div><div style='padding: 10px 0px;border: 1px solid transparent;'><div style='font-size:16px;word-wrap: break-word;'><H2 style='font-size: 1em; margin: 0px'><b>What STERIS Offers </b></H2></div><div><p><em>We value our employees and are committed to providing a comprehensive benefits package that supports your health, wellbeing, and financial future. </em></p><p><em> </em></p><p><em>Here is just a brief overview of what we offer: </em></p><ul type="disc"><li>Market Competitive pay</li><li>Extensive Paid Time Off and added Holidays</li><li>Excellent Healthcare, Dental and Vision benefits</li><li>Long- and Short-Term Disability coverage</li><li>401(k) with a company match</li><li>Maternity and Paternity Leave</li><li>Additional add- on benefits / discounts for programs such as Pet Insurance</li><li>Tuition Reimbursement and continuing education programs</li><li>Excellent opportunities for advancement in a stable long-term career</li></ul></div></div></div> <p>Pay range for this opportunity is $74,162.50 - $91,612.50. <span style="color:black">This position is eligible for bonus participation.</span></p><p> </p><p>Minimum pay rates offered will comply with county/city minimums, if higher than range listed.

Pay rates are based on a number of factors, including but not limited to local labor market costs, years of relevant experience, education, professional certifications, foreign language fluency, etc.</p><p> </p><p>STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: <a href="https://steris-corp-comm.box.com/s/pgvfuqq6urrtkov891ypp1a7bvdvn2ta">STERIS Benefits</a></p><p> </p><p>Open until position is filled.</p><p> </p><p>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 and life sciences products and services around the globe. For more information, visit <a href="https://www.steris.com">www.steris.com</a>.</p><p> </p><p>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.</p><p> </p><p>STERIS