| Position Requirement: |
| 主要职责：
1. 产品注册可行性评估，协助文件体系和质量管理体系的实施和维护;＆
2.负责编写和提交国内产品注册的文件;以及证书续期的工作（含香港和中国内地）;＆
3.跟踪注册文件的评审,准时回复注册评审中的问题；&
4.能够与官方及客户进行有效的沟通;＆
5.及时了解香港/澳门和中国内地的对于药品注册的监管要求和市场趋势，以评估政策的变更对公司业务的影响。
资历及经验：
教育背景: 科学专业大专以上学历;
1. 欢迎应届毕业生应聘此职位，本岗位上班地址香港柴湾;
2.相关经验较少的候选人将被考虑为助理品质保证主任;
3.熟练使用MS Office办公软件(Excel, Word, PowerPoint)及中英文文字处理;
4.熟悉香港中成药注册流程及具备相应经验者优先;
5.能立即到岗者优先;
6.工作努力、主动、自我激励、团队合作精神和快速学习能力。
公司福利：
每周工作5天（周一至周五：上午8点半至下午5点半）
绩效奖金
人寿保险
年假
带薪产假、陪产假和婚假
职业发展机会
在职培训 |
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