Quality Systems Specialist (Senior) - Manufacturing Industry | Medical Devices (ISO 13485 | 21 CFR Part 820)
- International Business
- Permanent role
- Attractive Package & Scope
My client is a well-known International Medical devices Business. They are currently looking to hire a Quality Systems Expert who will be responsible for ensuring the compliance of medical device manufacturing and quality systems processes.
Key areas of Focus : CAPA, Compliance Audits and Inspections, Site Assessment, Subject matter expert for Quality Systems and related documentation
This role requires a Degree holder with relevant hands on experience in quality management systems within the Medical Devices Industry. The ideal candidate should have experience and knowledge in ISO 13485, 21 CFR Part 820.
The role offers an amazing `opportunity to join a market leader in the Medical Devices Industry who is well known for their innovative products and solutions, along with an attractive package and amazing career prospects.
PS: Only open for candidates who are stationed in Singapore.
Please send your resume in WORD format by clicking the apply button below or contact Savi on +65 6701 1524 for a confidential discussion. Please note that only short-listed candidates will be contacted.CEI Reg. Number R1216080 (Sathiyarajan Vinayagamani).
