Position Summary
The 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. Quality Inspectors support manufacturing and servicing operations by performing incoming component and in-process product inspections using standard measurement equipment. They identify, segregate and document rejected material and participate in Material Review Boards to ensure the proper documentation and disposition.
They may also review other related Quality documentation such as device history or calibration records.
HOURS: Monday - Friday dayshift 6/7/8am start time + overtime as needed
PAY: $20-23hr + quarterly bonus & merit
LOCATION: 14605 28th Ave North Plymouth, MN
HIRE: Direct, full time.
What You'll Do
- ✓Conducts incoming component and in-process product inspections to approprite standards.
- ✓Identifies, segregates and documents rejected components and materials.
- ✓Participates on a Material Review Board to review and process non conformance reports.
- ✓Supports NC disposition activities such as re-inspection.
- ✓Enters and retrieves inspection and Nc data from local and global systems.
- ✓Reviews related Quality documentation such as DHR’s or calibration records.
- ✓Supports local problem solving activities and may identify opportunities for improvement.
- ✓Complete other duties as assigned.
Skills, Abilities, and Experience
Required
- ✓HS Diploma/GED + 1yr 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, generate detailed, high-quality documentation, work with others in analyzing and solving technical problems and perform/manage multiple tasks in parallel.
- ✓Ability to work in a professional manner to support team actions and effectively manages work tasks.
Preferred
- ✓Experience working in a Continuous Improvement (C.I.) or 5S environment.
- ✓Over 1yr of Quality Inspector experience at a Medical Device manufacturing/production company.
- ✓Experience with component inspection, specifically, in medical device production.
- ✓Previous experience documenting information in SAP or similar system.
- ✓Knowledge and working experience using calipers, rulers, and other metallurgy tools.
- ✓Keen eye for detail and process/procedure adherence.
Other
- ✓Lifting, pushing, pulling 25-50lbs.
- ✓Bending, walking, standing, sitting, typing, hand manipulation, visual acuity.
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 (bi-weekly).
- ✓Benefits after 30 days.
- ✓Extensive Paid Time Off and 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.
Pay range for this opportunity is $20hr - $23hr. This position is eligible for bonus participation.
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.
STERIS offers a comprehensive and competitive benefits portfolio. Click here for a complete list of benefits: STERIS Benefits
Open until position is filled.
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 www.steris.com.
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 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.