Validation Technician in Bradford

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 passionate about supporting the medical and pharmaceutical industries? Do you care about keeping patients and people safe? If so, then a career with Steris AST could be a great fit for you.

What is involved

• Contributes to the accurate and safe processing capability of the company by coordinating and scheduling all Customer validations and dose mappings.
• Calibrates and maintains proper function of data collection devices used in validations and qualifications.
• Investigates, analyses and reports procedures and provides solutions to process deviations and Customer complaints.
• Optimizes processing by coordinating scheduling of Customer product; assists plant management in training operations employees in performing process procedures.
• Provides Customer service by assisting in the performance and adherence to ISO 11135 and ISO 11137 requirements.
• Strives for continuous improvement by analysing new or alternative ways to improve operations.
• Contributes in a team effort by performing according to the guidelines outlined in the STERIS Code of Business Conduct, and other directives.
• Supports the STERIS AST business imperatives of Growth, Operational Excellence, Leadership Excellence and Customer Focus.
• Exhibits a commitment to the STERIS AST shared values of Customer Satisfaction and Continuous Improvement.

Customer Performance Qualification

• Follow all technical procedures and work instructions (local and global).
• Responsible for PQ Product incoming inspection.
• Execute the PQ dose mapping Plan (including dosimeter placement).
• Coordinate PQ treatment with Operation.
• Ensure PQ are performed on time according to planning defined.
• Report the status of PQ activities.
• Retrieval of dosimeters.
• Prepare documentation and product for collection.
• Report any Nonconformity or deviation during PQ activities.

Dosimetry System

• Responsible for dosimeters measurement used for PQ and OQ activities.
• Support routine dosimeters measurements.
• Responsible for reporting laboratory environment conditions.
• Perform the cleaning or performance verification of the laboratory equipment where required.
• Report any deviation or non-conformity.
• Support the management of site dosimeter stock (Incoming inspection, storage, consumption).

Required Experience

• A minimum of one (1) year of experience in sterilization or related industry.
• Ability to effectively write and verbally communicate in English.
• Effective interpersonal skills as demonstrated through prior experience.
• Ability to navigate through defined computer screens.
• Prior experience organizing and analysing, and utilising Level 2 math skills to determine organizational, Customer and regulatory problems and formulate corrective action plans.
• Prior experience working in a detailed environment.
• Normal hearing range sufficient to hear alarms, bells, horns, etc.
• Ability to occasionally work outside of normal business hours and at various locations.

Preferred Experience

• Associates Degree.

STERIS plc provides employment and advancement opportunities without regard to age, disability, gender reassignment, marriage or civil partnership, pregnancy and maternity, race, religion/belief, sex (gender), sexual orientation or any other legally protected characteristic as defined by UK employment law. The Company bases all employment decisions on merit, qualifications, skills, and abilities with the intention that the best candidate is selected for each position. STERIS is a leading global provider of products and services that support patient care with an emphasis on infection prevention.