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ISO 13485 Auditor

Job Information

  • Post Date:2018-02-16
  • Career Level:Middle
  • Location:Not Specified
  • Salary:HK$20,000 - 30,000 /month (negotiable)
  • Employment Type:Contract, Freelance, Full Time, Part Time, Permane
  • Job Function:Manufacturing & Production  Others  Quality Assurance, Control & Testing / ISO  

Job Description

Primary Responsibilities:

  • ISO management system audits in China, HK, Macau, and occasionally in other countries.
  • Optional technical or operational management roles will be offered to suitable candidates.
  • Optional training responsibility may be assigned.

 

Requirements:

  • Degree holder or higher.
  • 6 years' or more working experience in manufacturing industry, including
    4 years' or more experience in medical device manufacturing or its supply chain.
  • The candidate with such manufacturing experience in automotive industry can be considered for IATF 16949 automotive auditor instead.
  • Experience in railway, aerospace, chemical, mechanical, E&E industry, or their supply chain is advantage.
  • 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 QMS, ISO 14001 EMS, or ISO 45001 OHSMS Lead Auditor Training Certificates.
  • It’s an advantage, but not necessary, if qualified as 3rd-party auditor, such as ISO 13485, IATF 16949,  IRIS, ISO 27001, AS 9100, IRIS, OHSAS 18001, QC 080000, or ISO 22000 auditor.
  • It’s an advantage for candidates with experience in FDA, 21 CFR Part 820, MDR, IVDR, MDD, MDSAP, or other medical devices related regulations.
  • For suitable candidate, business development or management roles may be offered.
  • Either full-time, Part-time or freelance basis acceptable to us.
  • Candidates in Mainland China with required qualifications may apply, supported with immigration program.

 

Typical career path of our auditors can be found at http://dqs.hk/career

Company Info

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