About this role
## Position Summary
This is a Fixed Term Contract of 6 - 12 months
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.