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Quality Assurance Regulatory Affairs Manager (PC080604) | [²é¿´¸ü¶àÀàËÆÖ°Î»] |
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ְλÀà±ð£º Éú²ú/¼Ó¹¤/ÖÆÔì ¹¤×÷µØµã£º ±±¾© ·¢²¼ÈÕÆÚ£º 2008-06-27 ¹¤×÷¾Ñ飺 3-5Äê ×îµÍѧÀú£º ±¾¿Æ ¹ÜÀí¾Ñ飺 ·ñ ¹¤×÷ÐÔÖÊ£º ȫְ ÕÐÆ¸ÈËÊý£º 1ÈË Ö°Î»ÔÂн£º 15000-20000Ôª/Ô ְλÃèÊö/ÒªÇó£º Client Introduction: Our client is one of the world¡¯s largest medical device producers headquartered in Europe. Job Responsibilities: Responsible for all the regulatory requirements and company policies and procedures matters regarding environment, health, and safety. Establish and maintain quality management system documentation and all needed procedures. Ensure initial and continuous training of personnel for the consistent implementation of quality system requirements and procedures. Set up and review products¡¯ test plans and procedures and control all products quality records. Achieve or review all quality system related audits including sub-contractors, software development teams, equipment factory assembly and testing. Analyze and audit (external and internal) in order to define or re-establish yearly quality objectives. Monitor the effectiveness of the quality management system and follow-up the continuous process improvement projects and the key processes performance indicators. Qualifications/Requirements: Electro-mechanical Engineer or equivalent (Master degree in science is preferred). 3 years of practical experience as Quality Assurance Manger for a Company for which the quality management system was at least encompassing the requirements of the ISO 9001:2000. Qualified as Quality System Auditor for Mechanical and electrical design and manufacturing according to the requirements of the ISO 9001:2000. Communication and empowerment skills with positive mindset. English speaking and writing in addition to the Chinese How to apply: Please email your resume to resume.bj@adecco.com , stating the job title in the subject line. ÁªÏµ·½Ê½£º .
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