Validation Engineer

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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.

Position Summary

• Manages Customer Validations ensuring that all validation activities are carried out in compliance with Customer requirements, STERIS policies & procedures, ISO 11135, and ISO 13485, relevant international standards, directives, and regulations.
• Establishes strong Customer relations and provides exceptional Customer service to ensure Customer qualification requirements are met or exceeded throughout all stages of the validation.
• Proactively supports their direct Supervisor to successfully achieve departmental and site objectives and undertake assigned projects.
• Adopts positive cross‑functional relations. Liaises with quality, operations planning, laboratory and Customer Service to coordinate and progress Customer validations and projects.
• Collaborates with EO TechTeam to support the establishment of a best‑practice approach through knowledge sharing and providing recommendations for EO TechTeam harmonization.

Duties

Duties - cont'd

Education Degree

Bachelor's Degree in Engineering General or Science

Required Experience

Diploma / Degree in life‑science or Engineering with a minimum of 1 year industrial experience with knowledge of ISO 13485, process validation and Microbiological / chemical testing. Knowledge of EO sterilisation process and ISO 11135 desirable.

In lieu of meeting the minimum educational requirement, applicants with a minimum of 3 years industrial experience preferably in EO sterilisation, demonstrating strong technical skills with comprehensive working knowledge of quality standards ISO 11135 and ISO 13485 process validation and Microbiological / chemical testing associated with the EO sterilisation process will be considered.

Work Requirements

STERIS is an Equal Opportunity Employer.

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