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This company are leaders in there field and provide high tech solutions for areas such as Oncology and Neurology. They are known for there innovation and the high calibre products they provide. Lately there Neurology devices have been singled out for particular praise.
This is a broad role that will see the candidate establish processes for quality management systems across there European sites and also implement quality improvement programs to ensure regulatory compliance. As this role is a hybrid role the candidate will also have Regulatory duties that include but are not restricted to regulatory reviews of documentation, liaising with Regulatory bodies and providing RA guidance for Northern territories
The client would like to see applications from candidates with experience of Quality Audits and systems with a good exposure to Regulatory functions and the ability to provide Regulatory guidance to Nordic, Benelux and UK regions. A devices or diagnostics background is preferable but not essential.
On offer for this role is a salary of £35,000 to £40,000 with a package that includes a high bonus.
This is a broad and challenging role within a friendly working environment.
For more information about this role or to make a general enquiry about career opportunities please feel free to contact Stephen Kenny from the Quality team by e-mail to (see below)
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