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Lilly QA Assistant - Inspection in Suzhou Manufacturing-苏州, China

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 39,000 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.


Responsibility for Statistical Inspection:


-Ensures Good Documentation practices and compliance with inspection and operational related documents


-Complete manual visual statistical sorting inspection for Suzhou Parenteral products in alignment with production schedule, and also to finish the room clean base on the SOP requirements


-Document defect classification information within manufacturing ticket associated with statistical inspection


-Ensure appropriate sampling of final semi-finished product, delivering the samples to the appropriate laboratories and completing all associated documentation

其他 :



-Support Operational inspection personnel with completion of required training and qualification activities


-Support Operations and investigation related to appropriate classification of defects


-Develop process and equipment knowledge, in particular as it relates to the control strategy for cartridge filling

基本要求 :

Basic Requirement:


Associate degree or above, majored in pharmaceuticals, chemistry or related sciences.


One to three years of experience in production or QA or QC


Pass an annual vision test and be free of color blindness


Must be equivalent to 4.9 or above vision acuity(5.0 or above correctable vision acuity)


Strong Attention to detail


Root cause analysis/Troubleshooting skills and requires good communication skills


Additional Preference:


Experience in Production, Engineering, QC, QA, Technical Services, or Regulatory is desirable.


Overtime may be required.


During qualification, validation, and routine operations, will be required to wear pager or carry a phone for off- shift coverage and respond to operational issues.


Applicant may work in various areas within the Parenteral Plant. Some allergens are present in the Parenteral Plant. Mobility requirements and exposure to allergens should be considered when applying for this position.

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 ( ) 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.

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At Lilly we strive to ensure our employees are part of a team that cares about them and our shared purpose of making life better for those around the world. How do we do this? We continue to look for ways to include, innovate, accelerate and deliver while maintaining integrity, excellence and respect for people.​ We hope that you seek to join us on our journey as we create medicine and deliver improved outcomes for patients across the globe!