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

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

DUTIES

E-Beam Process Operator related (Routine & Validation Process)

• Management and recording of incoming Goods: Receive customer batches for processing, perform quantity and quality checks and complete associated batches records (electronic and paper records).
• Preparation of products for process,
• Ensure that all products are labelled correctly and informs the E-beam Supervisor of any discrepancies as and when they arise.
• Prepare dosimeters to routine and validation batches and maintain appropriate records.
• Place and retrieve routine and validation batches on and from the E-Beam conveyor and prepare product for shipping.
• Read routine and validation dosimeters and maintain appropriate records.
• Ensure that all products are labelled and identified correctly for shipping.
• Ensure that the E-beam Supervisor is informed of any damage that occurs throughout the E-Beam process.
• Assist with Shipping Goods: shipping of customer batches for processing, perform quantity and quality checks and complete associated batches records (electronic and paper records).
• Support E-Beam Technical Department in all activities relating to E-Beam and related equipment qualification and calibration. (e.g. Spectrophotometers, dosimetry, etc.)

OTHER RESPONSIBILITIES AND DUTIES

• Alerts E-Beam Supervisor or equivalent of any process related problems/incidents.
• Co-operate with environmental and personnel monitoring of radiation levels.
• Attends arranged medical examinations when required.
• In conjunction with the management team and Technical Department develop and implement systems ensuring best practice product traceability in the E-Beam processing of product.
• Assist and carryout specific projects required for production.