Quality Technician

STERIS IMS; Mentor (OH); On-site; USD 40,000 - 65,000; Full time

Job summary

An established industry player is seeking a Quality Technician to support quality functions and ensure compliance with regulatory standards. This role involves conducting QC tests, documenting non-conformances, and collaborating on problem-solving activities. The ideal candidate thrives in a fast-paced environment, possesses strong analytical skills, and is detail-oriented. Join a company dedicated to creating a safer world through innovative healthcare solutions, where your contributions will directly impact patient care and safety.

Qualifications

• Minimum of one year experience in manufacturing or repair environment.
• Ability to work under strict deadlines and generate high-quality documentation.

Responsibilities

• Conduct in-process sub-assembly and final QC acceptance testing.
• Assist in production line quality investigations and problem-solving activities.
• Identify and document product and process non-conformances.

Skills

Problem-solving

Documentation

Teamwork

Technical analysis

Detail-oriented

Excel proficiency

Word proficiency

Education

High School Diploma or GED

Tools

PC applications

Job description

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 Technician 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. The technician supports manufacturing and servicing operations by performing and documenting problem-solving investigations, conducting in-process sub-assembly and final QC product acceptance testing. They assist in identifying and documenting process and product non-conformances, review device history records, and execute calibration and environmental monitoring processes.

Duties

1. Conduct in-process sub-assembly and final QC acceptance testing.
2. Assist in production line quality investigations and problem-solving activities.
3. Investigate production line stoppages to identify corrective actions.
4. Identify and document product and process non-conformances.
5. Participate on a Material Review Board to review and process non-conformance reports.
6. Review device history records and support batch record release.
7. Enter and retrieve quality data from local and global systems.
8. Perform site calibration activities and recordkeeping.
9. Execute environmental monitoring processes and recordkeeping.
10. Complete other duties as assigned.

Education

• High School Diploma or GED

Required Experience

Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks.

Preferred Skills and Experience

• Ability to work in a fast-paced environment with strict deadlines.
• Ability to generate detailed, high-quality documentation.
• Ability to analyze and solve technical problems collaboratively.
• Teamwork: Collaborates effectively with others and supports team actions.
• Manages work tasks effectively, is detail-oriented, and strives for continuous improvement.
• Proficiency with PC applications, including Excel and Word.

STERIS is a leading global provider of products and services supporting patient care with an emphasis on infection prevention. We help our customers create a healthier and safer world by providing innovative healthcare, life sciences, and dental products and services. STERIS is a $5 billion, publicly traded company (NYSE: STE) with approximately 17,000 associates and customers in more than 100 countries.

If you need assistance completing the application process, please call 1 [phone]. This contact is for accommodation inquiries only and cannot be used to check application status.

STERIS is an Equal Opportunity Employer committed to diversity and inclusion in the workplace. We ensure recruitment, hiring, training, transfer, and promotion without regard to race, color, religion, age, disability, national origin, citizenship, military or veteran status, sex, sexual orientation, gender identity, genetic information, or other protected categories by law. Our policy reflects our commitment as a federal contractor and our core values of equal employment opportunity.