Quality Management Systems Officer, Medical Devices, Medical Device, Cambridge, Quality Management Systems Officer
This globally recognised market leader is a specialist in manufacturing, developing and supplying Medical Devices used in the diagnosis and treatment for cancer. This company has recently merged with one of the world largest organisations and have now created a new role for a Quality Management Systems Officer to join their team in Cambridge.
As the Quality Management Systems Officer you will be responsible for ensuring quality management systems are compliant to FDA and ISO standards. This will include responsibility for quality control at key stages of manufacture, goods inspections and final release to market.
Other duties within this varied role will include:
-Developing Quality Management Systems in response to changing business requirements
-Inspecting goods
-Quality assurance and Regulatory Affairs metrics data collation and reporting
-Quality System document control
-Management of non-conformance reporting system
The suitable candidate will have previous experience of working in a quality role within the medical device industry. Experience of working to ISO 13485, FDA and GMP standards is also required for this position.
The successful candidate will receive full training and on going career progression opportunities to further enhance your skills.
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