Job Description

Growing Fortune 500 medical devices organization Cross functional and regional collaboration Exciting career progression pathResponsibilities Maintains document management system and document control ensuring Good Documentation Practice such as document and record accuracy and completeness as well as security. Perform analysis of internal quality data and prepare management reports on quality metrics Conduct due diligence checks, evaluate batch documentation and ensure overall systems, products and processes to meet quality and relevant regulatory requirements. Lead the development and implementation of quality initiatives to address product, process and system inadequacies to achieve continual quality improvement objectives Maintain QMS and quality related activities eg. Change control, deviations, CAPA, customer complaints etc. Conduct internal and external audits as required Lead or support global and regional continuous improvement projects.Requirements At least 1 year of quality assurance working experience in pharmaceutical/medical devices industry Degree or diploma in science/engineering or relevant discipline. Working knowledge in implementation and maintenance of the ISO 13485:2016 standard Motivated and driven personalityFor more information, kindly apply with your CV in Word format or send to Ambrose Chan to have a confidential discussion on the position.Registration Number: R1218177 EA License Number: 17C8502
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