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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.
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.)
Duties - cont'd
Quality
* Maintain accurate and complete records of activities performed.
* Ensure that the documentation is completed to the highest standard as per company SOP’s etc.
* Attend required trainings,
* Notifies Supervisor or equivalent of any deviations or problems.
* Ensure your own training record is accurate, up to date and reflective of current practice.
Time Keeping and Attendance
* Ensure that timekeeping records are filled in on a daily basis and access control cards are swiped when entering and exiting facility.
* Ensure that the E-Beam Supervisor is informed if unable to attend work as per company sickness / absence policies and procedures.
Duties - cont'd
Dose Map Studies
* Assist E-Beam Production Technician with dose map activities as required.
* Ensure that all relevant paperwork is collated and presented to the E-Beam Technical Department.
General Housekeeping
* Ensure that the E-Beam area is kept to the highest standard at all times.
General Production Support
* Assist other production departments as required.
Duties - cont'd
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.
Education Degree
High School Diploma or GED
Required Experience
Please note that this position is a shift based role
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.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Management and Manufacturing
* Industries
Medical Equipment Manufacturing and Hospitals and Health Care
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