Primary Responsibilities:

• ISO management system audits in China, HK, and occasionally in other countries/areas.
• Training course development and deliveries.
• Optional technical or operational management roles will be offered to suitable candidates.

Requirements:

• Degree holder or higher.  (important)
• 7 years' or more working experience in manufacturing industry, including (important)
  4+ years' in medical devices supply chain for ISO 13485 auditor, or
  4+ years' in automotive supply chain for IATF 16949 auditor.
• Fluent written and oral English, Mandarin, and Cantonese. (Important)
• It’s an advantage for candidates with PECB, CCAA, DGQ, IRCA, or Examplar certified 5-day ISO 9001:2015 or ISO 13485:2016 Lead Auditor Training Certificate.
• It’s an advantage, but not necessary, if qualified as 3rd-party auditor, such as ISO 9001, ISO 13485, IATF 16949, IRIS, or ISO 27001 auditor.
• For ISO 13485 auditor, it’s an advantage for candidates with knowledge in FDA, 21 CFR Part 820, MDR, IVDR, MDD, or MDSAP.
• For IATF 16949 auditor, it’s an advantage for candidates with experience in APQP, FMEA, SPC, MSA, and PPAP.

Typical career path of our auditors can be found at https://dqs.hk/career. The remuneration scheme will include basic salary and extra audit days allowance.