亚检招聘体系审核员

You will be expected to:- Supervise our Manufacturing Audit programs.- Raise awareness of relevant Quality Management, and Manufacturing Process related issues among our clients and the QIMA Team, through formal training and relevant technical inputs.- Audit the manufacturing sites of our clients' suppliers, sometimes without warning. Your areas of attention will according to the applicable international standard or the client's in-house procedure.- Be alert to any violations, staying vigilant when dealing with factory management, and recording all your findings in detailed reports, to be delivered to the client.- Approach your job with utmost integrity, as your conduct during an audit can have lasting consequences for the supplier, factory staff, and our clients.It could be you if you have: > GMP professional for Pharmaceutical, Medical Devices, and Cosmetic Industries.> Experienced and certified auditor for ISO9001, GMP/ISO13485.> At least 5 years relevant working experience preferred.> Good Command of English (Spoken and written).职位招聘1人原标题：《工厂审核员 GMP Auditor 医疗器械类》