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)