Job Functions: International markets represent significant growth opportunities for the pharmaceutical industry and for Lilly. One key element of our strategy is to grow our international business and as a result, we need talented individuals from hi
务述: 1ç›é€‰åŒºåŸŸç‚¹çš„KOL客户,ç»ç®¡å’Œç»´æŠ¤ç‚¹10KOL+15个年医师,医生对产的认知处方观念 2é€šè¿‡é«˜è´¨çš„å¦æœ¯å†…å®¹å’Œé«˜æ ‡å‡†çš„æ‰§è¡Œæ±‚ï¼Œæ–é«˜å¦æœ¯ä¼šè®®çš„质,符区域推广ç–略,确产ç–略地 3自我的å¦ä¹ èƒ½åŠ›å’Œå›¢é˜Ÿç›®æ ‡ä¸€è‡´ ,良好的执行力å¦ä¹ 能力维逻辑性 ï¼Œæ˜Žç¡®å›¢é˜Ÿçš„ç›®æ ‡ï¼Œé€šè¿‡å¸‚åœºåˆ†çŽ°ä¸šåŠ¡å¢žé•¿ç‚¹ï¼Œåˆ¶å®šåŒºåŸŸå¸‚åœºç–ç•¥ åŠ¡èµ„æ ¼ï¼š 1本科或以上å¦åކ 2制业区域市场验或销售管验 3内分泌领域工作验优先 4具备较强的市场分能力,大客
主工作责: * 守注射剂工厂的安全政ç–å’Œç¨‹ï¼Œé€ ä¸€ä¸ªå®‰å…¨çš„å·¥ä½œçŽ¯å¢ƒã€‚ * å®ˆæ ‡å‡†ä½œç¨‹å’ŒåŠ¨ç”Ÿäº§ç®¡è§„èŒƒï¼Œä»¥ç¡®è´¨ã€‚ * 作自动/自动/人工视觉检测设备完产的检测,并按照批记录求记录作æ¥éª¤ã€‚ 求: * 专科以上å¦åŽ†ï¼Œå…·å¤‡è‡³å°‘3å¹´æˆ–ä»¥ä¸Šçš„åˆ¶é€ æˆ–åŒ…è£…éªŒï¼Œç†Ÿæ‚‰GMP求。 * 身体康,工作实,能够适应长时间检,长时间站立/走动工作模。 * 具有较强的å¦ä¹ 能力和实际作能力。 * 具有级英è¯èƒ½åŠ›ï¼Œè®¤è¯†
Development of Health Outcomes Research Studies: * Discuss and provide inputs regarding clinical plan, protocol design and follow-up of Health Outcomes Research Studies. * Effective and timely review and synthesis of published literature and pr
主能: 1. ä¸¥æ ¼å®ˆå·²æœ‰çš„æ”¿ç–程(安全,生产工艺,消毒,更衣ç‰ï¼‰ï¼Œç¡®æ‰€æœ‰ä½œå‘˜å®Œé€‚当的培è®ã€‚ 2. ä¸»åŠ¨ç§¯åœ°åŠ åˆ°åˆ¶é€ åŒºåŸŸä¸è‡ªå®¡è®¡ï¼Œè§‚察项,差的改善措施的实施。 3. 与到生产计划ä¸ï¼Œä¸Žä¸ªåŒºåŸŸä½œä»¥ç¡®è®¤è®¾å¤‡å’Œéƒ¨ä»¶çš„完整性。 4. 助出æ£ç¡®çš„员工展评估。 5. åœ¨ç”Ÿäº§çº¿ä¸Šä¾›æŠ€æœ¯æŒ‡å¯¼ï¼Œå»ºç«‹å¥½çš„æ¦œæ ·ã€‚äº†è§£ç¨‹è´¨ä½“ç³»å’Œç›¸åº”çš„çš„æŠ€æœ¯çŸ¥è¯†ï¼Œä¸ºçº¿ä¸Šå‘˜å·¥ä¾›æŒ‡å¯¼ã€‚ 6. 支PT完PVP的执行,包括收集一线的建议和实施好的作方法ç‰ã€‚ 基本求: 1. 制é€
TS/MS Engineer - SA 作为SA & Validation Joint角色,时支SAå’ŒValidation相关的工作: åˆ¶ä½œå®¡æŸ¥æ‰¹å‡†æ–‡ä»¶ï¼Œå¯¹ç›¸å…³æŠ€æœ¯æ–‡ä»¶å¦‚ï¼šæ›´æŽ§åˆ¶ï¼Œæ³•è§„æ–‡ä»¶ï¼Œå·®è°ƒæŸ¥ï¼ŒéªŒæ–¹æ¡ˆå’ŒéªŒæŠ¥å‘Šï¼Œæ ‡å‡†ä½œè§„ç¨‹ï¼Œå·¥è‰ºç¨‹æ–‡ä»¶å’ŒéªŒæ€»è®¡åˆ’çš„å‡†å¤‡ä¾›æŠ€æœ¯æ”¯ã€‚ Prepare, review, approve and provide technical support for preparation of relevant technical documents, a
The primary responsibility of the CRP is to provide expert medical expertise to all aspects of the local business, to ultimately enhance the customers experience in scientific interaction with Eli Lilly. The CRP responsibility includes development t
Primary Function/Purpose * Central Marketing Organization – Marketing Capability Key Responsibilities * Responsible for coordinating Marketing training sessions and community activities. * Assist developing materials (slides, visuals, vide
JOB DESCRIPTION JOB TITLE: Associate Director, Portfolio and Project Management DEPARTMENT: Lilly China Drug Development and Medical Affairs JOB TITLE SUPERVISOR: Director, Portfolio and Project Management Purpose: The purpose of the Associate Direct
负责物料供应商管程的建立和实施 Be responsible for establishing and implementing material supplier management program * 建立和维护供应商管程, ç¡®ç¬¦ç¤¼æ ‡å‡†å’Œä¸å›½GMP求 Establish and maintain supply management program to meet requirements of Lilly Standard and Chinese GMP.
Purpose: The purpose of Senior Regulatory Affairs Manager role is to develop regulatory strategy for responsible products and manage regulatory projects. When approved by team head, can have subordinate(s) in team. Sr. Manager with subordinate need t
This job is under LCDDMAC (Lilly China Drug Development and Medical Affair Center) focused on Autoimmune, a prospective critical therapeutic area of Lilly China. Lilly China is developing and entering this area with innovative medicine and strong pip
Responsibilities: 该岗作为工厂QAè§„ä¸“å‘˜ï¼Œéœ€ç¡®å…¬æ•´ä¸ªç”Ÿäº§è¿‡ç¨‹å’Œäº§å¾—åˆ°æŽ§åˆ¶å¹¶ç¬¦æ‰€æœ‰é€‚ç”¨çš„æ ‡å‡†ï¼›å®žæ–½å®¡è®¡è¿‡ç¨‹ä»¥ç¡®å®šæ•´ä¸ªç³»ç»Ÿç¬¦æ±‚ï¼›å¹¶æ±‚å¯¹å®¡è®¡è¿‡ç¨‹ä¸å˜åœ¨çš„问题或缺陷进行追踪和出改进。 This role serves as Site QA compliance specialist, need to ensure that products are controlled and will meet, throughout the whole process, a
* Execution: * Supervise and manage marketing program implementation. * Develop promotional materials, including detailing aid, group selling slides, etc. * Manage OPEX Accountable for OPEX management. * Cross-functional communication:
JOB DESCRIPTION JOB TITLE: Sr. Project Management Manager DEPARTMENT: Lilly China Drug Development and Medical Affairs JOB TITLE SUPERVISOR: Director, Portfolio and Project Management Purpose: The purpose of the Sr. Project Management Manager (P3) ro
REQUIREMENTS & QUALIFICATION •Education background: Master degree in health sciences with 2-3 years relevant clinical or therapeutic experience. Clinical medicine background is preferred. •Proficiency in written English (sufficient to read and unders
Primary Function/Purpose 负责河部分城市的市场销售和业务拓展; ç»åŸ¹å…»èƒ½ä¾›è¶Šå®¢æˆ·ä½“验的员工; 创建并鼓励团队自我 赋能高效执行的文化; 清晰地ç–略性维整资,制定区域销售ç–略和市场活动计划; 较强大客户管能力; ç»äº¤ä»˜ä¸šåŠ¡æžœï¼› Key Responsibilities è´Ÿè´£ç®¡æ‰€è¾–åŒºåŸŸå’Œäº§ç»„çš„é¡¹ä¸šåŠ¡ï¼Œåˆ¶å®šåœ°åŒºç›®æ ‡ï¼Œé”€å”®ç–略和展方; 负责区域的人员招,团队的展,员工绩效管和教导; ä¸¥æ ¼ä»Žå›½å®¶ä»¥å…¬çš„æ”¿ç–ï¼Œç¡®å›¢é˜Ÿçš„è§„æ€§ï¼Œå¦æœ¯æ€§ï¼Œ
ç»Ÿè®¡å¦æ£€æŸ¥æ±‚: Responsibility for Statistical Inspection: -确良好的文件行为,符检作文件求 -Ensures Good Documentation practices and compliance with inspection and operational related documents -生产计划求,完州工厂的人工目视检查的工作任务,以完SOP所求的房间清 -Complete manual visual stat
Key Responsibilities ​ Be responsible for Diabetes products registration and relevant device * Under the general direction of supervisor, independently perform product registration and other activities. * Participate in the development of regul
Purpose: The purpose of the Medical Information Specialist role is to work with cross-functional, multidisciplinary teams to facilitate the creation of medical information about company products to answer unsolicited requests from internal business p
Primary Responsibilities: Provide regulatory expertise to propose China registration strategy through working closely with China and global study team and get alignment. Implement, review and update regulatory strategy when necessary. Ensure product
Development of Health Outcomes Research Studies: * Discuss and provide inputs regarding clinical plan, protocol design and follow-up of Health Outcomes Research Studies. * Effective and timely review and synthesis of published literature and pr
自动化工程师将负责制定实施和æ–å®Œå–„å·¥è‰ºè‡ªåŠ¨åŒ–è§£å†³æ–¹æ¡ˆï¼Œä¸ºç”Ÿäº§ä¾›çŽ°åœºæ”¯ï¼Œå¹¶ä¸Žç›¸å…³ç³»ç»Ÿè°ƒè¯•ç¡®è®¤ç»æ”¹å–„以故障处。这一求有生产工艺设备程代和控制系统技术(包括软件/硬件和现场仪表)方的专业技能。确自动化方案/系统控满足商业需求且符相关规范。 The Engineer - Automation is responsible for development, implementation, and continuous improvement of automati
主工作述: * 包装维护技术员主负责为包装生产过程供一线维修和维护支,ä»¥å·¥ç¨‹æ”¹é€ å®žæ–½ï¼Œ 包括: * 供生产设备日常巡检; * ä¾›è®¾å¤‡ç»´æŠ¤åŠ¡ï¼ŒåŒ…æ‹¬é¢„é˜²æ€§ç»´æŠ¤ï¼Œçº æ£ç»´ä¿®ä»ªè¡¨æ ¡éªŒç‰å·¥æ‰§è¡Œ; * 维护技术员主为产线供机器的故障维修务,必时汇报工程师寻求支; * 备件管:助备件在仓库收货,清点,盘库,备件清更新; * 支和执行生产设备更,程改善项目,与设备确认确认工作; * 和轮人员(作人员,维修专员,QAç‰ï¼‰
备注:雇于级型的员工(例如:P1-P3R1-R2B1-B3 ç‰ï¼‰ä»¥å…¶å½“çº§åˆ«ä¼ è¾“ï¼Œå°½ç®¡ä½œä¸šå¸ƒä¸æŒ‡ç¤ºäº†è¯¥çº§åˆ«ã€‚举个例,如果为 P1-P3 级型选择了 P2 候选人,则候选人在新角色ä¸çš„级别为 P2。 负责产的技术转移,技术更(例如ç»å·¥è‰ºæ”¾å¤§ï¼‰ï¼Œå¹¶ä¸ºæ³•规注册供支。 Responsible for product tech transfer, including other tech agenda management such as scale-up and sup