Validation Technician

Day to Day Activities (70%) 
• Works as directed by direct Supervisor to facilitate and support Customer EO qualifications within the EO 
Technical department. 
• Carries out all aspects of their role and associated documentation in compliance with STERIS Quality 
Management System, ISO11135, ISO13485 and FDA regulatory requirements while adhering to GMP and GDP 
requirement. Complies with local and global procedures. 
• Reviews qualification batch records for compliance to GDP and GMP, demonstrating a high level of attention 
to detail.  Follows up with Operations to address and close out on any batch record queries within agreed 
timelines.  
• Provides administration support to the EO Tech Team.  Completes filing and archiving of qualification batch 
records and supporting EO qualification documentation.  
• Sets and agrees annual GPS performance objectives with direct Supervisor.  Actively participates in 
performance management reviews in lin...