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I am looking to bring on board a Senior Regulatory Affairs consultant to support and develop a Quality department.
This position is within a leading Medical Device manufacturer in Oxfordshire, the have a wide portfolio range which is well established in the market for the reliability of their products.
The organisation is going through a phase of growth which isn't expected to slow any time thus the need to add resource.
This is a great opportunity to develop your career across a cross functional Quality Department. The pre requisites for this position are as follows;
Experience within Medical Device standards, FDA, ISO 13485
Time spent as an Internal Auditor
Knowledge of Regulatory affairs and Quality Management Systems
A strong communicator who can articulate to various stakeholders,
Experience within a Manufacturing Environment is desirable.
The salary for this position is negotiable on experience and will be accompanied with an excellent benefits package.
If this position is of interest please reply with an up to date CV and your salary expectation or contact me for further details.
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