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.

As a Quality Technician at STERIS, you will be 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. You will support manufacturing and servicing operations by assisting in performing and documenting problem-solving investigations and conducting in-process sub-assembly and final Quality Control product acceptance testing. Quality Technicians assist in identifying and documenting process and product non-conformances.  You will work with operations team members to perform and document problem-solving investigations. In addition, Quality Technicians may review device history records, authorize release of finished product/processes and execute calibration and environmental monitoring processes. This is a second shift position; 2:00pm - 10:30pm Monday - Friday.

What you'll do as a Quality Technician

•    Assist in production line Quality investigations and associated problem-solving activities.
•    May coordinate and conduct in-process and final QC product acceptance testing, depending on facility.
•    Investigate production line stoppages to identify corrective actions. 
•    Identify and document product and process non-conformances. Participate on a Material Review Board to review and process non-conformance reports.
•    Review DHR’s and support batch record release.
•    Enter and retrieve Quality data from local and global systems.
•    Perform site calibration activities and recordkeeping.
•    Execute environmental monitoring processes and recordkeeping.
•    Verify calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release.
•    Complete other duties as assigned.

The Experience, Skills, and Abilities Needed

Required:

• Minimum of one (1) year of experience in a manufacturing or repair environment or other technical production tasks with an associate degree. Will accept 3+ years of experience in lieu of degree.  
• Experience working in an ISO regulated environment.
• Ability to work in a cleanroom (Class 5 or Class 8) environment with strict deadlines.
• Proficiency using MS Excel.
  

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 a brief overview of what we offer: 

•            Market Competitive Pay
•            Extensive Paid Time Off and (9) paid Holidays
•            Excellent Healthcare, Dental and Vision Benefits
•            Long/Short Term Disability Coverage
•            401(k) with a company match
•            Maternity and Paternity Leave
•            Additional add-on benefits/discounts for programs such as Pet Insurance
•            Tuition Reimbursement and continued education programs
•            Excellent opportunities for advancement in a stable long-term career

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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, life sciences and dental products and services. STERIS is a $5 billion, publicly traded (NYSE: STE) company with approximately 17,000 associates and Customers in more than 100 countries.

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 and the use of affirmative action programs 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.

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