eli lilly and company Jobs & Career

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： 1筛选区域点的KOL客户，续管和维护点10KOL+15个年医师，医生对产的认知处方观念 2通过高质的学术内容和高标准的执行求，断高学术会议的质，符区域推广策略，确产策略地 3自我的学习能力和团队目标一致 ，良好的执行力学习能力维逻辑性 ，明确团队的目标，通过市场分现业务增长点，制定区域市场策略 务资格： 1本科或以上学历 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策和程，造一个安全的工作环境。 * 守标准作程和动生产管规范，以确质。 * 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步骤。 求： * 专科以上学历，具备至少3年或以上的制造或包装验，熟悉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。 * 具有较强的学习能力和实际作能力。 * 具有级英语能力，认识

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. 严格守已有的政策程（安全，生产工艺，消毒，更衣等），确所有作员完适当的培训。 2. 主动积地加到制造区域中自审计，观察项，差的改善措施的实施。 3. 与到生产计划中，与个区域作以确认设备和部件的完整性。 4. 助出正确的员工展评估。 5. 在生产线上供技术指导，建立好的榜样。了解程质体系和相应的的技术知识，为线上员工供指导。 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等。 基本求： 1. 制造

TS/MS Engineer - SA 作为SA & Validation Joint角色，时支SA和Validation相关的工作： 制作审查批准文件，对相关技术文件如：更控制，法规文件，差调查，验方案和验报告，标准作规程，工艺程文件和验总计划的准备供技术支。 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, 确符礼标准和中国GMP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QA规专员，需确公整个生产过程和产得到控制并符所有适用的标准；实施审计过程以确定整个系统符求；并求对审计过程中存在的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； 续培养能供越客户体验的员工； 创建并鼓励团队自我 赋能高效执行的文化； 清晰地策略性维整资，制定区域销售策略和市场活动计划； 较强大客户管能力； 续交付业务果； Key Responsibilities 负责管所辖区域和产组的项业务，制定地区目标，销售策略和展方； 负责区域的人员招，团队的展，员工绩效管和教导； 严格从国家以公的政策，确团队的规性，学术性，

统计学检查求: 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断完善工艺自动化解决方案，为生产供现场支，并与相关系统调试确认续改善以故障处。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,以工程改造实施， 包括： * 供生产设备日常巡检; * 供设备维护务，包括预防性维护，纠正维修仪表校验等工执行; * 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，QA等）

备注：雇于级型的员工（例如：P1-P3R1-R2B1-B3 等）以其当级别传输，尽管作业布中指示了该级别。举个例，如果为 P1-P3 级型选择了 P2 候选人，则候选人在新角色中的级别为 P2。 负责产的技术转移，技术更（例如续工艺放大），并为法规注册供支。 Responsible for product tech transfer, including other tech agenda management such as scale-up and sup