supervise operators to produce qualified pharmaceutical products in accordance with gmp, ehs
and other regulatory regulations, accomplish the production assignment on time; responsible for
work on documentations(including sop, batch record and data analysis etc); give training to
workers; timely take correct actions to the abnormal issues in production
管理一線操作人員按照gmp、ehs及其它法規的要求，生產出符合質量要求的藥品，按時完成生產任務；負責文件
方面的工作包括sop、批記錄和數據分析等；對下屬員工進行培訓；及時、正確處理生產過程中發生的異常情況

product/brand reference point
? have expertise in and knowledge of products, patient treatment trends, clinical trials and scientific activities within relevant disease area(s) and must continuously ｕｐｄａｔｅ this expertise and knowledge

external expert manager
? develop and maintain contacts with external experts based on their expressed needs to further understand and gain both insight and/or input into treatment patterns, including but not limited to:
1 the scientific activities taking place within the relevant disease area(s) 2 the needs and treatment trends of healthcare providers
? utilizes therapeutic expertise in contacts with external experts, to further understand and gain insight into:
1 treatment patterns
2 the scientific activities taking place within the disease area(s) 3 the needs and interests of healthcare providers
4 the medical needs of patients

contributor to customer focused activity
? involve in developing scientific presentations (e.g., abstracts or articles based on secondary data) under the guidance of the dah/das/msm manager which presentation should be reviewed according to the appropriate internal review processes to ensure medical accuracy and ethical and legal compliance
? propose or conduct scientifically meaningful medical programs such as continuous medical educational program, symposia, round ｔａｂｌｅ meeting, and advisory board meeting etc.

support & trainer
? prepare and/or contribute as appropriate to the initial and ongoing medical / scientific disease area and product-specific training of internal bms customers (sales force, etc) – in collaboration with the training department, if any - enabling the sales representative to understand and convey the scientific information of a brand appropriately in a medical accurate and compliant manner
? liaise with the medical information team to provide ongoing scientific and medical support to the business, in particular by responding to queries

contributor to brand plans & strategies
? contribute to the development of brand plans and strategies by communicating his or her medical insight and knowledge derived from healthcare providers or scientific publications about the product or disease area, in particular with reference to patient needs and treatment trends
pharmacovigilance

clinical trial/survey involvement
? provide feedback to medical data operation (mdo) on investigator sponsored applications and assist mdo in providing feedback to investigators
? provide input to dass on trial and survey feasibility and site suitability, based on knowledge of the field
?for investigator sponsored research, refers all questions regarding review status, review process or outcome to the mdo protocol manager
? may support bms sponsored research activities as listed in related directives

communicator of medical information
? presents approved scientific data of varying levels of complexity to healthcare providers in both group and one-to-one settings
? provides appropriate response and documents the provision of accurate, approved scientific data in response to unsolicited scientific questions or requests posed by healthcare providers for approved products/brands and for products in development
? shares medical insights reports in a timely manner with the matrix teams and other internal personnel

leading compliance & integrity culture

leading self
? is responsible for ｄｅｌivering optimal performance & results, balancing speed, quality and risks while in compliance with company’s code of business conduct and appropriate sops.
? is responsible for continuous self development, dedicate him/herself and engage others to achieve the organizational & team goals.
? participates in professional development activities to keep ｕｐｄａｔｅd to best practices, proactively seeking for new information/knowledge/resources and captures ａｄｄitional opportunities for development, shares the relevant information with peers and manager timely.
? promotes the company image by building up and keeping good reputation, providing professional service to the customers and stakeholders and by developing efficiency of the company processes and procedures.

1.deploy rountine maintenance activity，knowledge of cgmp and sass gmp requirement。
開展日常設備維修活動，了解cgmp及公司目前對gmp的要求。

2. develops equipment specifications and acceptance tests, and maintenance procedures for new or rebuilt equipment.
建立新增或大修設備接受流程，并建立相應的維修管理程序。

3. conducts failure modes and effects analysis (fmea) to ensure proper maintenance tasks and intervals are established for all equipment, systems and components in the rcm program.
執行fmea項目來確保在rcm項目中每臺設備都建立起適當的維修保養任務和頻次。熟悉設備控制設備的工作原理，熟練使用計算機進行設備數

4. develops equipment specifications and acceptance tests, and maintenance procedures for new or rebuilt equipment.
建立新增或大修設備接受流程，并建立相應的維修管理程序。

5. prepares reports to describe the status, benefits and opportunities within the rcm program to ensure strategic maintenance goals are being met.
匯報rcm項目的執行狀態，收益和機會，并確保會達到既定的rcm維修管理目標。

6. performs root cause failure analysis (rcfa) for equipment failures and identifies corrective actions necessary to increase future reliability.
對設備故障進行根源故障分析，并制定相應預防措施來提高可靠性。

7. periodically reviews maintenance equipment history in order to provide proactive solutions to potential problems affecting reliability and or cost.
定期審核維修保養記錄，并為會影響設備可靠性和高維修費用的潛在問題提出預測性維修解決方案。

8. works directly with the maintenance teams to provide guidance and decision making regarding the maintenance procedures and process in order to ensure the reliability goals for the site are met.
和維修團隊一起制定維修流程和規范，以保證達到工廠可靠性目標。

9. supports maintenance and operations for corrective and reactive maintenance as well as proactive maintenance related to reliability.
在參與預測性維修的同時，支持現場維修。

10. supports the ｅｘｅｃution of capital projects.
支持執行固定資產項目。

11. ensures ehs and gmp practices and regulations are considered in all maintenance activities.
確保所有維修活動和文件符合ehs和gmp規范。

12. lead the standardization of equipment, components, installation and technologies within all site major systems.
領導主要系統設備、部件、安裝和技術標準化。

13. ensures predictive maintenance efforts to attend routes, troubleshooting and corrective activities as needed.
確保預測性維修應用到維修活動的各個方面。

14.participate in shift working
需參與翻班維修工作（8小時早中夜班翻班工作制）