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Global device compliance specialist

Cork
beBeeCompliance
Compliance specialist
Posted: 25 January
Offer description

Our company is seeking a Regulatory Affairs Associate to manage regulatory submissions ensuring our devices are compliant with standards.


About the Role

* This position involves managing and coordinating all aspects of regulatory submissions including preparing, submitting, and maintaining records as required by relevant regulations
* Regulatory affairs experience in medical devices or related fields is highly valued
o Experience working with FDA or equivalent bodies
o Familiarity with applicable laws and regulations for medical devices
Career development opportunities available for motivated individuals who demonstrate excellent skills in this area


Benefits Package:

We offer an attractive benefits package that includes career growth opportunities,
extended health insurance plans, flexible work arrangements.

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