TS/MS Intern

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.

Organization Overview:

协调并管理文件及培训的状态及追踪，并根据需要支持TS/MS的相关技术文件的准备和翻译以及执行操作。

He/She is responsible to track TS/MS documents and activities when needed. Support TS/MS relevant technical documents preparation and translation as well as executions as needed.

Responsibilities:

• 协调管理TS/MS入职培训计划及追踪，包括但不限于更衣，物料传递等。Coordinate and manage and track TS/MS on boarding program, including but not limited to gowning and materials transfer.
• 负责TS/MS部门的文件管理，包括但不限于包括文件号码发放、编写、翻译、建立审核批准流程、文件审计追踪审核、文件回收及归档等工作。TS/MS document management, include but not limited to the assignment of document number, document preparation, translation, creating document review and approval workflow, document audit trail review, document recovery and archiving.
• 作为TS/MS部门知识管理，促进部门内员工知识和能力的整合和增强。Serve as the TS/MS knowledge management to facilitate the integration and enhancement of knowledge and capability
• 直接或间接参与生产设备和系统的验证，包括方案和报告的编写、翻译、数据处理以及执行操作的必要协助。Involve directly or indirectly in production equipment or system validation, including the document preparation and translation and provide support in execution activities.
• 负责TSMS非GMP耗材的管理工作，包括但不限于物料采购，物料盘点等。TS/MS non-GMP consumables management, including but not limited to materials procurement, materials inventory check, etc.
• 完成主管安排的其他工作Finish the other duties assigned by supervisor
• 接受主管的委派Accept delegation from supervisor.
• 遵守HSE各项管理流程，履行安全生产职责要求。Follow various HSE management procedures and fulfill the work safety responsibilities.

Additional Skills/Preferences:

• 具备独立工作的能力。Demonstrated ability to work independently.
• 具备GMP实践经验者更佳Practical GMP working experience is a plus
• 具备注射药物生产经验更佳Parenteral manufacturing experience is a plus

Additional Information:

• 申请人将工作于胰岛素笔芯无菌生产工厂的不同区域。Applicant will work in various areas within the Insulin Cartridge Parenteral Plant.
• 能每天从周一到周五工作8小时。Ability to work 8 hours’ days- Monday through Friday.
• 能够根据要求加班并能及时对应生产出现的问题。Ability to work overtime as required and available off shift to respond to operational issues.
• 会被要求合理数量的出差。Reasonable amounts of travel will be required

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.