I am currently representing a leading global biopharmaceutical company, looking for an ambitious individual within validation to join their site in the North Weston a full time, permanent basis.
You will be responsible for maintaining the qualified status of facilities, utilities and equipment on site, as well as acting as a CSV subject matter expert. Additionally, you will be required to provide expertise in the resolution on non-conformances and liaise with vendors and contractors onsite. You will also have exposure to and involvement with capital projects onsite.
This is an excellent opportunity to work on a growing biologics manufacturing site currently in an exciting period of significant growth and investment. To find out more or arrange a confidential discussion about opportunities, please complete the form below, or email firstname.lastname@example.org