REGULATORY AFFAIRS || MEDICAL DEVICES
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Regulatory Affairs professional with hands-on experience in medical device regulations, including ISO 13485 certification, QMS documentation and EU MDR compliance for CE. Also experienced in the cosmetics industry, managing new product dossiers and handling import applications through the Sugam portal.
Regulatory Affairs professional with hands-on experience in medical device regulations, including ISO 13485 certification, QMS documentation and EU MDR compliance for CE. Also experienced in the cosmetics industry, managing new product dossiers and handling import applications through the Sugam portal.
M.PHARM (QA) || CERTIFIED IQA
