Process Operator
2 weeks ago
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.
Position SummaryE-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.).
- 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.
- 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.
- 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.
- 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 carry out specific projects required for production.
STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention. STERIS strives to be an Equal Opportunity Employer.
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