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Quality Inspector

STERIS Healthcare United States

Conroe (TX)

On-site

USD 40,000 - 60,000

Full time

3 days ago
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Job summary

Join a leading global provider in healthcare as a Quality Inspector. In this role, you will ensure compliance with various regulatory standards through inspections and documentation. Your efforts will contribute to a healthier and safer world by supporting manufacturing and servicing operations. This position requires attention to detail and the ability to work collaboratively in a fast-paced environment.

Qualifications

  • Ability to work in a fast-paced environment with strict deadlines.
  • Ability to generate detailed, high-quality documentation.

Responsibilities

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

Skills

Teamwork
Problem Solving
Detail-oriented

Education

High School Diploma or GED

Tools

Excel
Word

Job description

Join to apply for the Quality Inspector role at STERIS Healthcare United States

At STERIS, we help our Customers create a healthier and safer world by providing innovative healthcare and life science product and service solutions around the globe.

Position Summary

The Quality Inspector is responsible for assisting in the administration of quality functions at a site to ensure 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 proper documentation and disposition. They may also review related Quality documentation such as device history or calibration records. The work schedule for this position is Monday - Friday, 1:30 PM - 9:30 PM.

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

High School Diploma or GED required.

  • 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.
  • Ability to perform/manage multiple tasks in parallel.
  • Teamwork: Collaborates with others and works professionally to support team actions.
  • Effectively manages work tasks, is detail-oriented, and strives for continuous improvement.
  • PC experience and familiarity with common desktop applications including Excel and Word.
Additional Information

STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. We are committed to creating a healthier and safer world through innovative healthcare, life sciences, and dental products and services. As a $5 billion publicly traded company (NYSE: STE) with approximately 17,000 employees and customers in over 100 countries, we value diversity and equal opportunity.

If you need assistance completing the application, please call 1 (440) 392-7047. This contact is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer, committed to affirmative action and ensuring equal employment opportunities regardless of race, color, religion, age, disability, national origin, citizenship, military or veteran status, sex, sexual orientation, gender identity, genetic information, or other protected categories.

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