Stay updated on current MDA guidelines and incorporate them into training modules.
Support participants in grasping key concepts of ISO 13485 : 2016 and related quality management standards.
Requirements
Extensive knowledge of GDPMD compliance and Malaysian Medical Device Authority (MDA) requirements.
Proven experience as a trainer or compliance auditor in the medical device sector.
Familiarity with ISO 13485 : 2016, medical device import / export regulations, and post-market requirements.
Strong presentation and communication skills with the ability to simplify complex regulatory topics.
Certification in GDPMD auditing or HRDcorp accredited trainer is an advantage.
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Selangor • Shah Alam, Selangor, Malaysia
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