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Validation Engineer - Leeds, United Kingdom - Planet Pharma
Description
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Validation Engineer (Commissioning) - Globally field based - Global Chemical Manufacturing
Location: Anywhere in the UK
Length: Permanent
Rate: Incredible salary and benefits
FTE: Full time
My client is a Chemical Manufacturing company seeking a Validation Engineer. This is a REALLY interesting role - I have just fully qualified with the line manager. Their business is growing rapidly in UK, Europe, North America and in the Far East. They wish to maintain this momentum by appointing a Validation Engineer to take on new global projects.
Background:
Requirements:
Must come from a GMP/Pharma environment
Experience of commissioning and validation procedures and documentation
Must have broad customer exposure/come from a customer facing role.
Know how to convey information to various stakeholders.
Knowing how to adapt communication style
If you would like to discuss this vacancy further or to discuss your career options in confidence, please email me on: -
If this role isn't suitable for you, please let us know if you can refer anyone – any recommendations are much appreciated Planet Pharma offers a competitive referral scheme so you will be rewarded for your help
About Planet Pharma
Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering. Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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