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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.
HOW YOU WILL MAKE A DIFFERENCE
Do you want to spend your working time making a difference in the world around you? Are you passionate about supporting the medical industries? Do you care about keeping patients and people safe? If so, then a career with Steris could be a great fit for you.
At STERIS, we are the trusted experts and global leaders in medical device repair services and surgical instrument manufacturing.
We are dedicated to enabling patient safety and driving improvements in quality outcomes and efficiency across all our products and services.
What is involved
* Assist in production line quality investigations and associated problem-solving activities.
* Perform inspection of Rigid and Flexible Endoscopes.
* 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 DHRs 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 final product release.
* Complete other duties as assigned.
Required Experience
* Ability to work in a fast-paced environment with strict deadlines.
* Ability to generate detailed, high-quality documentation.
* Ability to work with others in analyzing and solving technical problems.
* Teamwork: Collaborates with others and supports team actions professionally.
* Effectively manages work tasks, is detail-oriented, and strives for continuous improvement.
* Proficiency with PC and familiarity with common desktop applications including Excel and Word.
* Minimum 1 year of experience in a regulated manufacturing or repair environment or other technical production environment.
* Ideally, experience in Quality Inspection.
* Educated to a good general standard with strong verbal and numerical abilities.
* Basic end-user IT skills to operate track and traceability IT systems.
Preferred Experience
* TVQ or NVQ Level 2 in Decontamination or equivalent experience.
* Previous experience in Sterile Services and/or health-related products.
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 aim of selecting the best candidate for each position.
STERIS is a leading global provider of products and services supporting 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.
Job Segment: Infection Control, Industrial, Maintenance, QC, Healthcare, Manufacturing, Quality
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