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    • permanent
    • full-time
    About The Company. A medical devices company with presence globally. About The JobYou will be supporting the quality systems to ensure substantial ISO 13485 compliance. Also, you will be responsible for following up on post market surveillance activities and thus resolve quality issues via the CAPA system to pursue continuous improvement of the Quality System.This individual will be delivering the Quality management system training as well responsible for maintaining and establishing the QMS. In addition, you will be involved in post vigilance, active internal and external audits that comply with ISO 13485 & ISO 9001. About The Manager/teamThis position reports to the Manager for Quality Assurance and this role will be an individual contributor. Skills & Experience RequiredYou must be equipped with at least a Degree in Lifesciences, Engineering or equivalent.You must have at least 3 years in the medical devices and experiences in ISO 13485 regulation. To apply online, please click on the appropriate link. Alternatively, please contact Cyndi Chin on 6510 3656 quoting Ref No. 91M0160324EA: 94C3609 / R1215243
    About The Company. A medical devices company with presence globally. About The JobYou will be supporting the quality systems to ensure substantial ISO 13485 compliance. Also, you will be responsible for following up on post market surveillance activities and thus resolve quality issues via the CAPA system to pursue continuous improvement of the Quality System.This individual will be delivering the Quality management system training as well responsible for maintaining and establishing the QMS. In addition, you will be involved in post vigilance, active internal and external audits that comply with ISO 13485 & ISO 9001. About The Manager/teamThis position reports to the Manager for Quality Assurance and this role will be an individual contributor. Skills & Experience RequiredYou must be equipped with at least a Degree in Lifesciences, Engineering or equivalent.You must have at least 3 years in the medical devices and experiences in ISO 13485 regulation. To apply online, please click on the appropriate link. Alternatively, please contact Cyndi Chin on 6510 3656 quoting Ref No. 91M0160324EA: 94C3609 / R1215243

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