Description
Detailed list of main areas of responsibility:Commissioning and Qualification of critical utilities including -
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
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
This is an urgent requirement with competitive hourly rates. If you would like to apply please contact Sarah Irvine on . We also offer £200 worth of vouchers for any successful referrals.