Description
Our Specialist Pharmaceutical client is introducing a unique medical device to the market and is looking for a Quality/Validation Engineer to join their growing company.The successful candidate will represent our client in two separate UK based manufacturing sites, from Formulation and Aseptic filling, to the assembly and testing of the device in another location.
As a Quality/Validation Engineer you will be responsible for, but not limited to, the following:
Co-ordinating and managing CMO's, ensuring delivery on time and in budget
Answering queries from vendors and troubleshooting to avoid delays
Interfacing with Quality organisations and working independently as client representative
Driving project to completion and working with vendors to meet deadlines
Requirements:
Strong experience in a regulated Medical Device manufacturing environment
Quality/Validation Engineering experience within a new aseptic filling line or packaging line installation
An extensive background in Quality/Validation within a CMO or multiple site project and interfacing with Quality organisations
Experience with design through to commercialisation of a medical device desired
If you are looking to join this fantastic company, please apply today with an email highlighting your key skills and relevant experience aligned to this opportunity.