Job Description
Permanent
£50,000 + Benefits
West Sussex
A leading medical device manufacturer is seeking an experienced Validation Manager to join them on a permanent basis. The successful candidate will be responsible for establishing, managing and implementation of the validation programme.
The role shall develop to perform validation training, policies and procedures to ensure best practices are consistently performed. The position shall also support the clients business objectives, corporate policies, and world class manufacturing.
To be considered for the role you shall have a Science degree or other relevant degree or qualification. You will preferably be Lean Sigma trained & certified with good practical experience of its use both in QA & Manufacturing environments.
Knowledge of FDA regulations 21 CFR Part 820 & Part 11 & validation requirements, European Medical Device Directives and International standards, such as ISO 13845 (Medical Device Standard).
The successful candidate will have Validation experience with Process Validation, Test method Validation, Equipment Qualification, CSV Computer Systems Validation, Cleaning Validation and Sterilisation Validation
In order to be considered please forward your CV to harrison.s.a4ljeb7h174@entechts.aptrack.co.uk or call Harrison on 01442 898 900.