A challenging ,rewarding position has arisen within a Harlow Essex CM20 M11 based well established Medical Device company for a Quality Engineer . The company manufacture a wide range of unique products for the Medical industry and due to continued growth plus restructuring they are recruiting across a range of vibrant key roles .
Is for a experienced Quality Engineer with a Medical Device Regulatory Market /or Manufacturing background
So what's needed from you be to be considered ?
Experience in Medical Device industry is desirable.
Capable of continual improvement and CAPA programme.
Can you approve and implement validation documentation.
Show aspects of Product CE marking and US submissions experience.
Have knowledge of the medical device directive.
Do these key regulatory environment elements
Does CE US CAPA MDR ( MDD ) indicate your work history know how ?
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