Global Regulatory Specialist (EU MDR, ISO 13485)
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Accelero
Pontypridd
A global medical device company in Pontypridd is seeking a Regulatory Specialist to manage product Technical Files and support regulatory compliance across international markets. The ideal candidate has a degree in a scientific discipline and at least 1 year's experience in Regulatory Affairs, with strong knowledge of EU MDR and UK regulations. Additional benefits include 33 days of holiday,... |
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3 hours ago
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