岗位职责：
1、 了解gmp法规，了解cgmp及公司目前对gmp的要求；
2、 熟悉设备管理的规章制度；
3、 执行设备故障分析，制定改进预防措施；
4、 熟悉和了解各种制药设备，能按照 gmp 规范从事本公司所有要求的各种制药设备维修和预防性维护工作；
5、 确保所有维修和维护保养工作符合ehs规定；
6、 能区分各类设备中不同零部件的重要程度，并能作出判断，提出备件计划；
7、 及时发现并消除设备潜在风险；
8、 保证生产设备的安全、正常运行；
9、 参与新设备的安装、调试和验证，熟悉设备的使用；
10、 有较强的理解能力的工作总结能力；
技能要求：
1、 专科及以上学历，主修电气及自动化相关专业；
2、 具备相关电气操作相关证件，以及一定的英语读写能力；
3、 熟悉湿法制粒线、混合机、胶囊填充机、压片机、包衣机、泡罩包装线、瓶装线等生产设备；
4、 对维修和预防性维护的执行有丰富的实践经验；
5、 熟悉电气控制原理和siemens plc，具有五年及以上制药行业现场电气维修维护相关经验；
6、 具备电气图纸阅读能力和使用常用办公软件的能力；
7、 熟悉fema分析，能进行实际操作；
8、 自我激励的个人贡献者，具有全面的维修故障解决能力以及良好的团队合作精神，认真负责，沟通能力较强。

main responsibilities:
· support to cultivate and foster a culture of integrity within the
company;
· partner closely and interact effectively with internal clients to
understand business and provide business conduct guidance, counselling and
solutions to ａｄｄress challenges;
· support and ensure sufficient compliance support on innovative
business from screening of project ideas to ｄｅｌivery of final project results;
· monitor on regulatory requirements ｕｐｄａｔｅ and provide insights to
risks of potential relevance to the business;
· prepare regular reports of compliance activities in english & chinese
for management to review and analyze the risks in company operation;
· provide regular risk assessment for the business, design and implement
risk mitigation plans;
· monitor the companies’ activities and events to ensure the compliance
policy, procedures, and guiｄｅｌines are properly implemented;
· draft and review policies as needed.


requirements:
· bachelor’s degree or above required;
· above 8 years of working experiences in multinational companies with
comprehensive compliance and operational framework, rich experience in
compliance, internal control, or legal is a plus;
· experience in healthcare companies is preferred;
· profound knowledge in business practices and process improvement,
demonstrated ability to collaborate all levels of the organization, coordinate,
negotiate and influence various stakeholders for alignment;
· highly self-motivated, willing to take initiatives with good sense of
business acumen.
· strong knowledge of relevant laws, regulations, industry codes and
practices;
· ability to handle multi-tasks under pressure;
· strong written and verbal communication skills, project management
skills and analytical skills;
· fluent in english speaking and writing;
· some travel within prc is required.

responsibilities：
develop an understanding of regional and national scientific leaders and the healthcare environments in which they work through effective professional engagement with scientific leaders that are centered on science and credible exchange of unbiased scientific information.
interact with managed care organizations, healthcare professionals, clinical investigators, and other healthcare organizations providing fair, balanced, and scientifically rigorous medical and clinical information.
meet with healthcare professionals who might be interested in engaging in a scientific discussion regarding a product’s medical and clinical profile in the context of approved prescribing information as well as in response to unsolicited questions or requests for information which may involve off-label information. (unsolicited means that the information request was neither suggested nor encouraged by the msl or sales representatives)
participate in the development and implement tactics identified in the medical affairs plans (map).
work with clinical research personnel to identify potential investigators clinical research projects, based on the investigator’s expertise and access to appropriate patients.
alert investigators to company program for investigator initiated study proposals, working together with the medical manager on the process for submitting investigator designed proposals for review and approval; encourage and facilitate research publication of investigator initiated studies, in strict compliance with company policy and local ｃｏｕｎｔry regulations.
when requested (and consistent with local sops), may represent the medical department at local or regional medical events (e.g. medical congresses and symposia.)
facilitate the submission and publication of the study result from investigator initiated or company initiated projects.
qualifications：
candidates to possess a ｍａｓｔｅｒ degree in the life sciences (md, pharm.d, or pharmacist, biology) preferably with a specialization in the experience of oncology.
requires strong scientific baseline knowledge in therapeutic area, clinical trials methods, implementation and interpretation, sound scientific and clinical judgment, and eagerness to learn more in depth in therapeutic area.
strong, confident and engaging presentation skill, and capable for customer facing.
outstanding communication and skills and the ability to function within a team environment.
proactive