Job Description

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

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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

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Assists in production line Quality investigations and associated problem-solving activities.


Performs inspection of Rigid and Flexible Endoscopes


May coordinate and conduct in-process and final QC product acceptance testing, depending on facility.


Investigates production line stoppages to identify corrective actions.


Identifies and documents product and process non-conformances.


Participates on a Material Review Board to review and process non conformance reports.


Reviews DHR's and supports batch record release.


Enters and retrieves Quality data from local and global systems.


Performs site calibration activities and recordkeeping.


Executes environmental monitoring processes and recordkeeping.


Verifies calculations, dose ranges, dosimeter placements and special instructions prior to processing and part of final product release.


Complete other duties as assigned.

Required Experience

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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. Works in a professional manner to support team actions.


Effectively manages work tasks. Is detail oriented and strives for continuous improvement.


PC experience and working familiarity of 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 will have Quality Inspection experience


Educated to a good general standard with demonstrable verbal and numerical abilities.


Basic end user IT skills to operate track and traceability IT system.

Preferred Experience

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TVQ or NVQ Level 2 in Decontamination or equivalent experience. Previous experience in Sterile Services and/or health related products.

Skills

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Flexibility Teamwork Integrity Working under pressure Accountability Attention to detail





For more information about us, please visit our STERIS IMS website: https://www.steris-ims.co.uk/

Equal Opportunities

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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 17,000 associates and Customers in more than 100 countries.


STERIS strives to be an Equal Opportunity Employer.