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
About you: Do you want to spend your working time making a difference in the world around you? Are you motivated by impactful work? Do you have a passion for excellent quality, working with a variety of internal and external stakeholders, and possess strong customer support skills? If so, then a career with STERIS in our Healthcare team could be a great fit for you. About Us: At STERIS we are a leading global provider of products and services that support patient care with an emphasis on infection prevention. Our mission is to help our customers create a healthier and safer world. Working at STERIS, you
GROW ,
LEARN
and
MAKE A DIFFERENCE . We are currently recruiting for a Validation Analyst vacancy. This is an excellent opportunity to join us at a skilled level in a division that drives the business forwards through providing a best in class quality validation service to our customers. WHAT YOU WILL DO
The Validations Analyst/AP(D) is responsible for both the collation and the monitoring of quality, for all validation reports completed by the field service team, for all STERIS decontamination system equipment types. They are also to liaise with the sub-contracted Laboratories to expedite the delivery of results, and to clear and authorise invoices against our orders. They are to perform functions of an Authorised Person (Decontamination), where the customer requires a higher level of support, acting with full accountability to the customer. This role’s purpose is to support STERIS’s vision in creating a healthier and safer world by managing STERIS customer contract and non-contract needs and going above and beyond to meet our Customer’s expectations. Main purpose of the role is to collate full and accurate IP reports on completion of all validations carried out by STERIS field staff on decontamination equipment and as appointed STERIS company APD advise in accordance to testing International standards and national guidelines. Download and check engineer reports for precision and accuracy, liaise 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, liaise 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
Experience working in an office based customer service environment or sterilisation / decontamination administration environment. Comfortable with data analysis and numerical reasoning. Previous hands on or administration experience within decontamination environment. STERIS strives to be an Equal Opportunity Employer.
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About you: Do you want to spend your working time making a difference in the world around you? Are you motivated by impactful work? Do you have a passion for excellent quality, working with a variety of internal and external stakeholders, and possess strong customer support skills? If so, then a career with STERIS in our Healthcare team could be a great fit for you. About Us: At STERIS we are a leading global provider of products and services that support patient care with an emphasis on infection prevention. Our mission is to help our customers create a healthier and safer world. Working at STERIS, you
GROW ,
LEARN
and
MAKE A DIFFERENCE . We are currently recruiting for a Validation Analyst vacancy. This is an excellent opportunity to join us at a skilled level in a division that drives the business forwards through providing a best in class quality validation service to our customers. WHAT YOU WILL DO
The Validations Analyst/AP(D) is responsible for both the collation and the monitoring of quality, for all validation reports completed by the field service team, for all STERIS decontamination system equipment types. They are also to liaise with the sub-contracted Laboratories to expedite the delivery of results, and to clear and authorise invoices against our orders. They are to perform functions of an Authorised Person (Decontamination), where the customer requires a higher level of support, acting with full accountability to the customer. This role’s purpose is to support STERIS’s vision in creating a healthier and safer world by managing STERIS customer contract and non-contract needs and going above and beyond to meet our Customer’s expectations. Main purpose of the role is to collate full and accurate IP reports on completion of all validations carried out by STERIS field staff on decontamination equipment and as appointed STERIS company APD advise in accordance to testing International standards and national guidelines. Download and check engineer reports for precision and accuracy, liaise 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, liaise 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
Experience working in an office based customer service environment or sterilisation / decontamination administration environment. Comfortable with data analysis and numerical reasoning. Previous hands on or administration experience within decontamination environment. STERIS strives to be an Equal Opportunity Employer.
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