Validation Specialist
4 weeks ago
At STERIS, we strive to create a healthier and safer world by providing innovative solutions to our customers. As a Validation Specialist, you will play a crucial role in ensuring the quality of our decontamination systems.
About the Role
The Validation Specialist is responsible for collating and monitoring quality reports for all validation activities completed by our field service team. This includes liaising with laboratories to expedite the delivery of results and clearing and authorizing invoices against our orders.
Key Responsibilities
- Collate full and accurate IP reports on completion of all validations carried out by STERIS field staff on decontamination equipment.
- Download and check engineer reports for precision and accuracy, liaising with engineers and district service managers accordingly.
- Collate and analyze lab reports received following validation samples taken.
- Liaise with customers directly where results are out-of-specification.
- Monitor lab results and expected delivery dates, liaising with the laboratory where necessary to ensure results are delivered on time.
- Combine full IP reports, identifying these accordingly with lab result IDs, ensuring these reports are to the customer AE(D) and STERIS standards.
Requirements
1. Experience working in an office-based customer service environment or sterilization/decontamination administration environment.
2. Comfortable with data analysis and numerical reasoning.
3. Previous hands-on or administration experience within decontamination environment.
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.
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