Primary Responsibilities:

• EU MDR audits or training deliveries in different regions. 
• The standards may cover EU MDR, MDSAP, ISO 13485, etc, depending on the candidate' experience and qualifications.

Requirements:

• Degree holder or higher.  (important)
• 6+ years' working experience.
• 3+ years' experience in EU MDR associated with medical device manufacturing or CE mark application.
• EU MDR, MDSAP, MDD or ISO 13485 auditor qualification is an advantage.
• CCAA or HKICA registered ISO 9001 Auditor qualification is an advantage.
• Fluent in English and Chinese.
• Either employment or freelance approach.

For employed auditors, the remuneration scheme will include a basic salary and an extra audit days allowance. For freelance auditors, the service fee will be primarily based on audit days.

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