Description
Job Responsibilities:Detailed list of main areas of responsibility
Commissioning and Qualification of critical utilities including but not limited to:
DI Water
Compressed Air
Nitrogen
HVAC
Commissioning and Qualification of equipment and qualification of laboratory equipment
Commissioning and Qualification documentation generation, review and approval, where appropriate including:
Validation Project Plans
FMEAs/Risk Assessments
User Requirement Specification
Functional Design Specification
Factory Acceptance testing
Site Acceptance Testing
Commissioning Test Plans
IQ, OQ and PQ protocols and reports Investigations
Review of computer system validation documentation for upgrade to laboratory equipment software and utility PLCs
Education and Experience Required for Role
Essential :
Third Level Degree
Minimum of 5 years experience in the medical device/pharma industry in validation role
This is an urgent requirement with competitive hourly rates. If you are interested in applying please contact Sarah Irvine on or reply with a copy of your current CV.