Quality Assurance Technician I

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.HeaderPosition SummaryJoin a company where the work you do makes a difference! We are One Team with One Goal. At STERIS Applied Sterilization Technologies (AST), it's our philosophy and our way of doing business. Through a network of over 50 facilities globally, STERIS AST has been committed to providing contract sterilization services to the medical device, pharmaceutical, consumer, and industrial communities for over 40 years. Our irradiation and gas sterilization services ensure the safety of those who use these products, including our families, our friends, and ourselves. If you are looking to join a collaborative and innovative team in an essential industry, apply for our Quality Assurance Technician I position today! This position works Monday through Friday, 7:00 am to 3:30 pm and offers overtime potential based on business needs. The hourly pay rate starts at $17.00.Reasons you will love working hereThis is an opportunity to join a company that will invest in you for the long-term. STERIS wouldn't be where it is today without our incredible people, whom take true pride in their work. That's why we share in our success together by rewarding employees for their hard work. We do this by providing competitive base salary plus bonus (as applicable), comprehensive benefits package that includes medical, dental, vision, paid PTO and holidays, 401K with company match.What you will do with us: Review hard-copy Lab reports and Calibration reports Execute label review Execute IP receiving Execute DHR reviews. Education Degree High School Diploma or GED You will be a great fit if you have: Minimum 1 year Microsoft Office experience Ability to effectively read, write and verbally communicate in English Ability to work under guidelines and supervision Basic concepts of regulations and standards, including, but not limited to, U.S. FDA device QSR, GMP and CGTP regulations, ISO 13485 medical device standard, and ISO 17025 laboratory standard Willingness to demonstrate through daily activities a model of continuous quality system activity monitoring to ensure compliance to documented standards Attention to detail. Proficiency in defect detection. STERIS is a $3B, publicly traded (NYSE: STE) organization with approximately 12,000 associates worldwide and operates in more than 100 countries. If you need assistance completing the application process, please call 1 392.7047. 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.Nearest Major Market: Minneapolis Job Segment: Technician, Medical, QA, Quality Assurance, Quality, Technology, Healthcare