Position Summary

This is a Fixed Term Specific Purpose Contract of 9 - 12 months to cover Maternity Leave

The purpose of this position is to support calibration, equipment qualification and test method validation projects in a regulated environment.

Authorised to perform specific activities including:

develop, modify, verify and validate methods under guidance
analysis of results, statements of conformity and opinions / interpretations under guidance
report, review and authorise results

Duties

Support Qualification and Validation planning activities and attending daily / weekly meetings where required 10%
Create and execute validation documents – 15%
Create and execute URS, IQ, OQ, PQ, TMV, Risk assessments– 15%
Review data and generate reports – 15%
Review calibrations certificates – 20%
Cross train to calibration methods if required – 10%
Document technical review and approval – 15%
Support equipment and test method improvements – 10%

Duties - cont'd

Education Degree

Bachelor's Degree in Science or Engineering General

Required Experience

Working in a regulated environment (Med Dev, Pharma etc.)
Customer facing activities.
Hands on test development and execution
Science/Engineering
Excellent communication & technical writing abilities

Preferred Experience

Skills

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 and life sciences products and services around the globe. For more information, visit www.steris.com.

STERIS strives to be an Equal Opportunity Employer.

Validation Technician (FTC)

Job Description