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.

REQUIRED EXPERIENCE

• Bachelors degree
• 1-5 years of combined Manufacturing/Quality Engineering/Quality Systems experience or minimum of 6 months on-site STERIS internship or co-op experience.
• 1-5 years of experience with medical device or other regulated industries preferred.
• 1-5 years of experience working in an ISO certified environment required.
• ASQ, QSR or familiarity with QSR/GMP regulations preferred.
• Excellent problem-solving skills
• Focus on identification of potential issues and continuous improvement.
• Experience working on cross-functional teams and on own initiative.
• Demonstrated excellent organizational, oral and written communications skills.
• Must have PC experience, as well as working familiarity of desktop applications including Excel, Word, and PowerPoint.
• Experience with statistical analysis software and Visio preferred.
• Validation experience

STERIS PLC PROVIDES EMPLOYMENT AND ADVANCEMENT OPPORTUNITIES WITHOUT REGARD TO AGE, DISABILITY, GENDER REASSIGNMENT, MARRIAGE OR CIVIL PARTNERSHIP, PREGNANCY AND MATERNITY, RACE, RELIGION/BELIEF, SEX (GENDER), SEXUAL ORIENTATION OR ANY OTHER LEGALLY PROTECTED CHARACTERISTIC AS DEFINED BY UK EMPLOYMENT LAW. THE COMPANY BASES ALL EMPLOYMENT DECISIONS ON MERIT, QUALIFICATIONS, SKILLS, AND ABILITIES WITH THE INTENTION THAT THE BEST CANDIDATE IS SELECTED FOR EACH POSITION.

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 18,000 associates and Customers in more than 100 countries.
STERIS strives to be an Equal Opportunity Employer

Please refer the Job description for details