Responsibilities:

• Assist in Quality Assurance and regulatory-related activities;
• Involve in the regulatory inspection. Ensure our company product quality in compliance with relevant laws, regulations, specifications and product standard;
• Ensure proper submission of technical documentation to various regulatory agencies around the world;
• Develop, implement and maintain the quality management system;
• Conduct supplier evaluation and maintain supplier management program for starting materials and packaging material;
• Assist in preparation of documents, such as SOP, specification and product labels complying with local and export countries' regulations;
• Handle customer complaints and follow up action closely with the factory.

Requirements:

• Degree holder in Engineering, Science, Quality Management or related disciplines;
• At least 1 years of QA working experience in Optics or Medical device industries;
• Hand on experience on quality inspection, auditing ,and testing;
• Good knowledge of ISO 13485, CE, FDA, CFDA quality system regulation and other related quality assurance systems in medical device;
• Knowledge with quality tools e.g. SPC, Six Sigma Tool, FMEA etc.;
• Knowledge/experience in Optics/lens manufacturing and/or assembly will be an advantage;
• Proficiency in PC applications, including MS Office;
• Self-motivated, proactive and possess good communication skills;
• Good command of spoken and written English and Chinese; Putonghua is an advantage.

Attractive remuneration package with benefits including 5-day work week, bank holidays and medical insurance will be offered to the successful candidate.  For application, please email your full resume with expected salary and availability by "Clicking Apply Now"

Personal data will be used for recruitment purpose only and will be treated in strict confidence.