Quality System Compliance Auditor (Medical Devices, Global)

Global Quality System Compliance Auditor in a leading Medical Devices company

Your new company

Leading company in the Medical Devices industry

Your new role

  • Manage all phases of global quality system compliance audits for compliance against US and international regulatory requirements and standards (e.g. FDA and ISO).
  • Investigate potential compliance issues and advise management proactively; coordinate the resolution of subsequent corrective actions.
  • Develop, or participate in the development of, solutions to quality system problems of intermediate to high complexity aimed at improving business systems and compliance; may be the primary representative of Quality group on projects.
  • Manage information availability for global audits to sites as needed during inspections and audits.
  • Manage audit records within the company's software system to allow trending of outcomes.
  • Other duties as defined by manager.

What you'll need to succeed

  • 7 years of experience working in the medical devices, pharmaceutical etc industries
  • 3 years of internal audit experience in quality management systems, class 2 or class 3 medical devices
  • Experienced in ISO 13485 and 21 CFR 820 regulations

What you'll get in return

You will be part of a leading organization who values employees and have a structured career growth with development opportunities. You will also be compensated with attractive remunerations.

What you need to do now

If you're keen on pursuing this exciting opportunity, please send a copy of your CV (word document) to geraldine.tay@hays.com.sg or contact Geraldine at +6563030157

Hays Registration Number: 200609504D, EA License No: 07C3924, Registration ID No.: (R22105664)



Job Type
Scientific and R&D
Life Sciences

Talk to a consultant

Talk to Geraldine Tay, the specialist consultant managing this position, located in Singapore
#27-20 UOB Plaza 2, 80 Raffles Place

Telephone: +6563030157

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