Component Quality Inspector

Torrey Holistics; Minneapolis (MN); On-site; USD 28,000 - 32,000; Full time

Benefits offered by this job

Market Competitive Pay

Benefits after 30 days

Extensive Paid Time Off

Job summary

STERIS is seeking a Quality Inspector to support incoming component and in-process product inspections at our Plymouth, MN site. You will verify adherence to ISO 9001, ISO 13485, MDSAP, FDA standards, and document NCs.

Responsibilities include MRB participation, NC disposition support, data entry in SAP, and calibration review. A detail-oriented team player with Excel/SAP proficiency is essential. Full-time, dayshift with overtime when needed.

Qualifications

• HS Diploma/GED plus 1 year of mechanical inspection or technical production experience.
• Proficient with Excel and Word; able to generate detailed documentation.
• Ability to work under deadlines and solve problems with a team.
• Professional conduct to support team actions and manage tasks.

Responsibilities

• Conducts incoming component and in-process product inspections to applicable standards.
• Identifies, segregates and documents rejected components and materials.
• Participates on a Material Review Board to review nonconforming parts.
• 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 DHRs or calibration records.
• Supports local problem-solving opportunities and coordinates improvements.

Skills

Quality Inspection Experience

Weighing Raw Materials

Composite Materials & Repair

Component Inspection

ISO 9001

Medical Device

Microsoft Word

Education

HS Diploma/GED

Tools

Excel

SAP

Calipers

Micrometers

Job description

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.

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 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.

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.

You should be proficient in:

• Quality Inspection Experience
• Weighing Raw Materials
• Composite Materials & Repair
• Microsoft Excel
• Component Inspection
• ISO 9001
• Medical Device
• Microsoft Word
• SAP

Machines & technologies you'll use:

• Measurement Gauges
• Calipers and Micrometers
• SAP