Quality Inspector

STERIS Canada Corporation; St. Louis (MO); On-site; USD 40,000 - 60,000; Full time

Job summary

A leading global provider of healthcare and life science products seeks a Quality Inspector to ensure adherence to quality standards. Responsibilities include conducting inspections, managing rejected materials, and supporting quality documentation. The role requires attention to detail and problem-solving skills in a fast-paced environment.

Benefits

Healthcare

Vision

Dental

401K Match

Quarterly Bonuses

PTO

Company Holidays

Qualifications

• Minimum of one year of experience in mechanical inspection or technical production tasks.

Responsibilities

• Conduct incoming component and in-process product inspections.
• Identify, segregate, and document rejected components.
• Participate in Material Review Boards.

Skills

Analytical Skills

Problem Solving

Attention to Detail

Teamwork

Education

High School Diploma or GED

Job description

Position Summary

The Quality Inspector is responsible for administering quality functions at a site to ensure adherence to standards such as ISO 9001, ISO 13485, MDSAP, FDA 21 CFR Part 820/211, EU MDR, and other applicable regulations. They support manufacturing and servicing operations by performing incoming component and in-process product inspections using standard measurement equipment. They identify, segregate, and document rejected materials and participate in Material Review Boards to ensure proper documentation and disposition. They may also review related quality documentation such as device history records or calibration records.

Benefits

• Shift: 3:00pm-1:30pm Monday - Thursday (training on 1st shift, then move to 2nd shift)
• Healthcare, Vision, Dental, 401K Match, Quarterly Bonuses, PTO, Company Holidays

Duties

1. Conduct incoming component and in-process product inspections to appropriate standards.
2. Perform final inspection and product release.
3. Identify, segregate, and document rejected components and materials.
4. Participate in Material Review Boards to review non-conformance reports.
5. Support non-conformance disposition activities such as re-inspection.
6. Enter and retrieve inspection and NC data from local and global systems.
7. Review related quality documentation such as DHRs or calibration records.
8. Support local problem-solving activities and identify opportunities for improvement.
9. Perform other duties as assigned.

Education

• High School Diploma or GED

Required Experience

Minimum of one (1) year of experience in mechanical inspection or other technical production tasks.

Preferred Skills

• Ability to work in a fast-paced environment with strict deadlines.
• Ability to generate detailed, high-quality documentation.
• Strong analytical and problem-solving skills.
• Ability to manage multiple tasks simultaneously.
• Teamwork and professional collaboration.
• Attention to detail and continuous improvement mindset.
• Proficiency with desktop applications such as Excel and Word.

STERIS is a leading global provider of healthcare and life science products and services, committed to creating a healthier and safer world. We are an equal opportunity employer. For assistance with the application process, call 1 [phone]. This contact is for accommodation inquiries only.