Quality Inspector II

STERIS - Manufacturing Facilities

Plymouth, MN

JOB DETAILS
SKILLS
Administrative Skills, Calibration, Capability Maturity Model (CMM), Code of Federal Regulations, Computer Skills, Continuous Improvement, Desktop PC, Detail Oriented, Documentation, ERP (Enterprise Resource Planning), Engineering Drawing, Environmental Monitoring, FDA (Food and Drug Administration), FDA Requirements, Geometric Dimensioning and Tolerancing, Healthcare, ISO (International Organization for Standardization), ISO 9001, Instrumentation, Manufacturing, Manufacturing Operations, Medical Equipment, Microsoft Excel, Microsoft Word, Multitasking, Problem Solving Skills, Process Improvement, Product Documentation, Quality Control, Regulations, Root Cause Analysis, SAP, Safety Alerts, Standard Operating Procedures (SOP), Team Player, Time Management, Trend Analysis, Windchill PLM Software
LOCATION
Plymouth, MN
POSTED
4 days ago

Position Summary:

The Senior Quality Inspector is responsible for assisting in administration of the quality functions at a site to assure adherence to ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR and other applicable regulatory standards. The Senior Quality Inspector supports manufacturing and servicing operations by performing incoming component and in-process product inspections which are more complex requiring the use of sophisticated measurement systems and instrumentation. Senior Quality Inspectors identify and document component, process and product non-conformances and lead investigation/root-cause countermeasure activities. They work with operations team members to perform and document problem-solving investigations. In addition, Senior Quality Inspectors may oversee device history record reviews and manage calibration and environmental monitoring processes.

Hours:

6am - 2:30pm Monday through Friday

What You'll Do:

  • Conduct complex incoming component and in-process product inspections.
  • Participate in quality investigations and associated problem-solving/root-cause activities.
  • Support the creation of incoming inspection plans.
  • Identify and document product and process non-conformances.
  • Identify opportunity for process continuous improvement.
  • Participate on a Material Review Board to review and process non conformance reports.
  • May review DHR paperwork for completeness and accuracy against standards.
  • Track, trends and reports quality data for assigned areas.
  • May support site calibration activities depending on facility structure.
  • Complete other duties as assigned.

Skills, Abilities, and Experience:

Required:

  • Highschool Diploma or G.E.D. Equivalent.
  • Ability to read engineering drawings (specifications), interpret lines and GD&T symbols, and check dimensions and tolerances on raw materials.
  • Ability to read, understand, and follow verbal and written work instructions/SOPs and safety warnings labels.
  • Minimum of three (3) years of experience in mechanical inspection or other technical production tasks.
  • PC experience and working familiarity of common desktop applications including Excel and Word.
  • Ability to work in a fast-paced environment with strict deadlines
  • Ability to generate detailed, high-quality documentation.
  • Ability to work with others in analyzing and solving technical problems.

Preferred:

  • Basic knowledge of GD&T (Geometric Dimensioning and Tolerancing).
  • Previous experience working in ERP (Enterprise Resource Planning) Systems. Specifically: SAP, Windchill, and/or Trackwise, etc.
  • Experience working in a regulated environment having to adhere with ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR regulations.
  • Previous expereince using measurement equipment like: Calipers, Drop Gauges, Micrometers, etc.
  • Expert ability to read and comprehend complex specifications and S.O.P.s.
  • Previous experience working in as a Quality Inspector in the medical device manufacturing or related industries.

Other:

  • Ability to perform/manage multiple tasks in parallel.

  • Ability to collaborate with others and work in a professional manner to support team actions.

  • Effectively manage work tasks with attention to detail while striving for continuous improvement.

  • Ability to lift, push, and/or pull 25-50lbs.

  • Temperature controlled, warehouse environment.

What STERIS Offers:

We value our employees and are committed to providing a comprehensive benefits package that supports your health, well-being, and financial future.

Here is just a brief overview of what we offer:

  • Market Competitive Pay
  • Extensive Paid Time Off and (9) added holidays
  • Excellent Healthcare, Dental and Vision Benefits
  • Long/Short Term disability coverage
  • 401(k) with company match
  • Maternity & Paternal Leave
  • Additional add-on benefits/discounts for programs such as Pet Insurance
  • Tuition Reimbursement and continued educations programs
  • Excellent opportunities for advancement and stable long-term career

You should be proficient in:

  • ISO 13485
  • FDA Regulations
  • ISO 9001 Certification Experience

Machines & technologies you'll use:

  • Coordinate Measuring Machine (CMM)
  • Calipers and Micrometers

About the Company

S

STERIS - Manufacturing Facilities