Description
The successful candidate will have experience in the following: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 pharma industry in validation role.
Very good interpersonal, communication and presentation skills, along with an ability to deliver on targets and deadlines.
If you are a Validation Engineer with over 5 years of industry experience then please contact Sarah Irvine on or alternatively forward me a copy of your up to date CV.
If this does not sound like the opportunity for you, but you are a Validation/Quality professional within the Pharmaceutical industry, please feel free to get in touch, to see what other opportunities we may have available.