Description
An exciting new opportunity has become available for a Validation Engineer in a market leading medical device firm. Candidate's responsibilities will be to support assigned projects and will required expereince of writing and executing IQ's, OQ's and PQ's. Quality Responsibilities;*Candidate's responsibilities will be to support assigned projects and will required expereince of writing and executing documents.
* Provide support to production and R&D ensuring new and existing products and equipment meet the companies' current validation requirements.
* Liaise with other departments to ensure the processes and procedures needed to maintain validated systems are established, understood and implemented. Quality Requirements; * Expertise in the validation of modern analytical techniques
* Experience in the validation of manufacturing processes and the associated scale up activities
* Audit consultant experience in ISO13485, MDD93/42/EEC & ISO9001 If you are interested in this role, have any questions about this position or would like to register your interest in other positions, please feel free to send your up to date CV or contact me on .
To find out more about Real please visit www.realstaffing.com