Quality Specialist

Welcome to the Latest Job Vacancies Site 2025 and at this time we would like to inform you of the Latest Job Vacancies from the Steris with the position of Quality Specialist which was opened this.

If this job matches your qualifications, please send your application directly through our latest Job site. Indeed, every job is not easy to apply because it must meet several qualifications and requirements that we must meet in accordance with the standard criteria of the Company who are looking for potential candidates to work. Good job information Quality Specialist below matches your qualifications.

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 Specialist 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. This role coordinates document control transactions, site record retention, calibration and inspection activities.  In addition, the Quality Specialist will facilitate Customer complaint investigations, assist in audit coordination, support supplier quality and customer assessments and support risk management activities where appropriate.  This role may also track and trend Quality data and support the site Management Review process.

What You'll do as a Quality Specialist

•  Complete document control transactions.•  Manage Customer complaint investigations and complete complaint documentation.•  Facilitate CAPA and NCR investigations and may coordinate investigation documentation.•  Review DHR's and support batch record release.•  Manage record retention practices within the site.•  Manage site calibration activities and recordkeeping.•  Support site inspection activities and recordkeeping.•  Coordinate internal and external audits.•  Support supplier quality and Customer assessment activities.•  Track and trend site Quality data.•  Support targeted Lean activities.•  Complete other duties as assigned.

The Experience, Skills and Abilities Needed

Required:

• Associates degree
• Minimum two (2) years of experience in quality in a regulated environment (i.e FDA/ISO 13485).

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) added 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.

How to Submit an Application:

After reading and knowing the criteria and minimum requirements for qualifications that have been explained from the Quality Specialist job info - Steris Mentor, OH above, thus jobseekers who feel they have not met the requirements including education, age, etc. and really feel interested in the latest job vacancies Quality Specialist job info - Steris Mentor, OH in 2025-06-10 above, should as soon as possible complete and compile a job application file such as a job application letter, CV or curriculum vitae, FC diploma and transcripts and other supplements as described above, in order to register and take part in the admission selection for new employees in the company referred to, sent via form this bottom.