Description
I am currently working with one of the world's largest Clinical Research Organisation who is looking for a Quality Assurance Advisor to join their team. You will initially be working on a 6 month contract in Macclesfield, Cheshire.As a Quality Assurance Advisor, you will have a focus on Good Manufacturing Practice (GMP). You will have a broad range of responsibilities to ensure that activities and processes in Pharmaceutical Development functions and the R&D supply chain comply with Regulatory requirements, Good Manufacturing Practices and the client's internal quality system requirements.
Your key skills / experience will include:
> Scientific degree with at least 3 years experience of working within a pharmaceutical GMP environment,
>Broad understanding of Quality Systems and GMP > Understanding of the pharmaceutical/drug development process
> Good communicator with experience of interacting effectively across interfaces > Experience preferably within a pharmaceutical development organisation
> Fluent in written and spoken English
If you fit the profile outlined above and you would like to discuss further, please send in your updated CV and call Nighat Rehman on .
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