Are you a Validation Specialist with experience in equipment, utilities and facilities? I have an opportunity for a Validation Specialist to join a global organisation in Liverpool on a contract basis.
About the role:
Length - 3 months
Inside of scope for IR35!
You will join the project and assist with projects in an ever-changing role.
- You will support the design and C&Q of GMP pharmaceutical equipment.
- You will be responsible or the full validation lifecycle Inc. IQ, OQ, PQ, URS, FAT and so on.
- You will be responsible for facilities, utilities and associated computer systems.
You will have extensive pharmaceutical or biological manufacturing experience. You will have strong skills within commissioning, qualification and validation.
your application has been submitted