Associate-Quality Assurance

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

• Be primarily responsible for product verification and physical checks after products are received into the MIC warehouse, on a batch-by-batch basis. 主要负责产品进入MIC仓库后，按批次开展产品验收及实物核对。

• Perform timely batch release in both SAP and WMS after product verification. 产品验收完成后，及时在SAP系统和WMS系统中完成批次放行。

• Promptly report and provide feedback to the MIC Quality Manager if any quality issue or suspected counterfeit product is identified, and work with the team to manage and resolve the issue. 如发现任何质量问题或可疑假药情况，应及时向MIC质量经理报告并反馈，并与团队共同处理和管理。

• Receive and verify returned products and hand them over to the MIC Quality Manager for disposition. 负责退货产品的收货与验收，并移交MIC质量经理进行判定。

• Verify the accuracy of serialization codes before uploading them to the website. 复核上传至网站的追溯码准确性。

• Download and verify product transportation temperature data. 负责产品运输温度数据的下载与审核确认。

• Maintain batch-release documents and related records. 维护批次放行相关文件及记录。

• Investigate and manage deviations/events that may potentially impact product quality and ensure that such deviations/events are handled in accordance with Lilly GSOP requirements. Effectively follow up on corrective and preventive actions to ensure implementation and completion. 开展并管理可能影响产品质量的偏差或事件，确保相关处理符合礼来GSOP要求；有效跟进纠正和预防措施，确保其落实并完成。

• Lead and/or participate in quality improvement initiatives or CAPAs to enhance the overall quality system or compliance level of the warehouse. Activities may include SOP revisions, change controls, and other project- or system-related improvement activities. 主导和/或参与质量改进项目或CAPA，以提升仓库整体质量体系或合规水平。相关活动可包括SOP修订、变更控制，以及其他项目或系统相关的改进活动。

• Perform other tasks assigned by the supervisor. 完成主管分配的其他工作任务。

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