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 35,000 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.
岗位描述/Position Brand Description:
Participate in clean utility system monitoring and microbiological lab tests, meanwhile ensure the monitoring and the test operations are complied with both Chinese GMP and Lilly GQS requirements.
Apply HSE Procedure correctly and wear the expected PPE correctly during work.
Apply Data Integrity requirement correctly during work.
Share event on quality and HSE inside and outside team actively.
Perform quality monitoring for clean utility systems, including portable water system, purified water system, water for injection system, clean steam system and pharmaceutical compressed air system.
Perform QC microbiological lab release testing, include but not limited to: Utility, IPC, excipients and PPC.
To assist with method verification and study for microbiological lab test (including protocol draft, method verification execution, report generating).
Be responsible for the SOP draft/revision in QC microbiological lab.
Participate in microbiological lab clean room management.
Participate in management of consumables, reagents, and global /local standards which related to microbiological lab test.
Participate in document management for microbiological lab.
- 负责实验室日常报告的第二人复核 （可选）
To be responsible for the routine lab reports second person verification.
- 负责实验室新进人员的培训 （可选）
Responsible for fresh analysts’ training.
Participate in 5S management for microbiological lab.
To assume other tasks related to Quality.
To assist with GLIMS deployment.
To assist with lab quality system continuously improvement and GLIMS deployment.
College degree or above, majored in pharmaceuticals, biological or related sciences.
Capable of writing and read in English.
Understanding of Good Manufacturing Practices.
Overtime may be required.
Working on shift may be required.
Eli Lilly and Company, Lilly USA, LLC and our wholly owned subsidiaries (collectively “Lilly”) are committed to help individuals with disabilities to participate in the workforce and ensure equal opportunity to compete for jobs. If you require an accommodation to submit a resume for positions at Lilly, please email Lilly Human Resources ( Lilly_Recruiting_Compliance@lists.lilly.com ) for further assistance. Please note This email address is intended for use only to request an accommodation as part of the application process. 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.
To submit resume, visit https://www.lilly.com/careers and apply to Req ID R-29648.
Lilly is an EEO/Affirmative Action Employer and 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.
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