Your new company
A leading pharmaceutical manufacturing organisation is seeking an experienced CQV / Validation Engineer to support a programme of new asset introduction and qualification activities within a GMP regulated environment. Working alongside Engineering, Quality, Manufacturing and Project teams, you'll play a key role in ensuring critical equipment, facilities and utilities are introduced and maintained in a validated state.
Your new role
As the Validation Engineer, you will be responsible for delivering qualification and validation activities across laboratory and manufacturing systems. Key responsibilities will include:
What you'll need to succeed
Desirable experience:
Must have Full Right to Work in the UK for duration of contract. No Sponsorship provided.
What you'll get in return
What you need to do now
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
