This position is responsible for conducting audit/technical documentation review in Active Medical Product (AMP) of Central region.
1.Conduct auditing/technical documentation review according to standard requirements, regulatory requirements, procedures and code of conduct;
2.Maintain customer communication as project leader for the allocated customers;
3.Support relevant in AMP field for customer service and complaint investigation;
4.Perform other duties assigned by active auditing supervisor and section manager.
1.Bachelor degree or above;
2.At least 4 years working experience in the field of medical device;
3.At least 2 years quality management working experience;
4.Know well about all company’s policy, procedures related to medical business, with qualification as medical device in certain area;
5.Respect and safeguard company’s image, reputation and benefit;
6.Diligence, self-motivation, self-improvement and strong teamwork spirit;
7.Good communication and interpersonal skills;
8.Can work independently and efficiently, can work under pressure;
9.Good computer skill;
10.Good command of English;
11.Physical condition allows normal working, stable outputs and business trip as required.