Description
Job Responsibilities:Commissioning and Qualification of critical utilities including:
DI Water
Compressed Air
Nitrogen
HVAC
Qualification of equipment and laboratory equipment
Commissioning documentation generation, review and approval.
Validation Project Plans FMEAs/Risk Assessments
User Requirement Specification
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:
Third Level Degree in relevant science or engineering discipline.
Minimum of 5 years experience in the medical device/pharma industry in a Validation/Quality role.
Very good interpersonal, communication and presentation skills, along with an ability to deliver on targets and deadlines.
Proficient in the use of MS Office and Chromatography systems software.
If you are interested in this role or require further information please contact Sarah Irvine directly on .