Description
My client is looking for Validation Engineers to drive the development of its regulatory compliance services business area, which delivers a range of regulatory services throughout the UK and overseas.Ideal candidates will have a validation background, experience in the pharmaceutical or medical device industries, and a good working knowledge of GAMP®, GxP, validation, risk management and 21 CFR Part 11. A "can do" positive attitude is required with the desire to extend your skill set, take on board new challenges and help the company grow its reputation and customer base.
Variety
The work will be varied and every validation project will be a new and exciting opportunity to use and develop different skills.
In this role you will be responsible for delivering my clients portfolio of computer, process and equipment validation services.
Desirable Skills
Knowledge of automated equipment validation experience AND some understanding of software validation is an optimal background for this role.
Essential Skills
A good understanding of either the pharmaceutical or medical device industry is essential. You must also have experience in carrying out validation activities, adhering to GxP guidelines, and meeting the FDA's rule, 21 CFR Part 11.
Excellent attention to detail is essential and the individual must be competent in the creation of documentation including validation master plans and reports, and confident in carrying out testing and qualification activities, such as pre-delivery testing, IQ, OQ and PQ.
Applicants must be able to communicate effectively both formally and informally, orally and in written English.
Locations
Norfolk
Salary
The salary is competitive.