Italy Job Openings

STERIS

Quality Technician

Seriate

FULL TIME

September 20, 2024

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

We are looking for a Quality Technician to join our Quality team based in Seriate (BG). To implement the Quality Management System in Seriate e Beam site under the supervision of the Site QA Supervisor and in collaboration with QA Team Italy.

Duties

1.To review batch documentation after processing and to ensure that errors, problems and anomalies are fully investigated and documented.
2.To be responsible for conforming product release for all processes at site.
3.To ensure Quality System in Production is in compliance with STERIS Procedures, Standards and any Applicable Laws.
4. To initiate, investigate, control and analyze non-conformance reports, to ensure corrective action, in collaboration with all departments involved, is implemented and that it is effective.
5.To initiate, investigate, control and analyze the recording and investigating of Customer
6.To support the Site QA Supervisor and the QA Team, in conjunction with the technical groups, to verify the conformity of all process validation documents (PQ) and in collaboration with Validation Department and the Site QA Supervisor, to ensure the need for validation is identified and ensuring that the appropriate action is taken.

Duties - cont'd

7.To develop, support and maintain the Production Employee Training Program about Quality Guidelines.
8.To identify and report any failures in the implementation of the quality system to the Site QA Supervisor, Country Quality Manager ITA and Operations Management.
9.To support and facilitate Audits. Ensure that the internal audit program is executed as per plan and perform audits as required
10.To monitor Production and Quality performance periodically and provide a report to all Departments of Seriate site on a regularly scheduled basis; monitor day to day CAPA reporting to ensure timely closure.
11.To support the Site QA Supervisor and the QA Team to implement continuous improvement activities in agreement with the Plant Manager.
12.To control, ensure that each new Local Working Instruction drafted agrees with STERIS Policy and QMS, in collaboration with the Site QA Supervisor and the QA Team, Production and Tech Team; to assist all Departments in their application.

Education Degree

Bachelor's Degree in Science or Biological Science

Required Experience and Competencies

Good level of English reading, writing and speaking communication skills
Full availability to travel
Preferable and appreciable knowledge in ISO 13485, ISO 11137, GMP and Quality Management
Team work attitude
Knowledge in Microsoft Office applications (Word, Excel, Access and Power Point).
Full time role, in case of needs, the person should be flexible in his/her time schedule

Additional Information

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, sex, sexual orientation, gender identity, genetic information, and any other category protected by state or local law.

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.
STERIS strives to be an Equal Opportunity Employer.

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