To formulate, implement and review work procedures to ensure effectiveness and efficiency to meet quality and regulatory requirements.
To ensure high level of compliance to ISO 13485, EU MDR 2017/745, MDSAP regulations and other relevant national authorities requirements in all assigned areas.
To support the documentation of CVM GDPMD system to ensure its compliance to MY-MDA requirements.
Requirements:
Degree in Engineering, Life Sciences or equivalent.
EA License No: 22C1414 Reg No.: R23113314
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