Lilly Posted June 16, 2026

Associate-QA Compliance

Suzhou, Shanghai, China FULL_TIME
Quality Associate

Lilly is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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.

岗位描述 Position Description:

该岗位为工厂合规QA,负责通过构建、完善、执行和监督质量流程来保障工厂质量体系的全面合规性。持续监督本地法规、药品生产质量管理规范以及礼来公司全球质量准则要求的实施,并按适当的管控措施及时上报潜在合规性风险。

This role serves as site Compliance QA, is responsible to ensure the overall compliance of the site quality systems by building, improving, executing and monitoring strong quality process. To monitor for compliance with local regulations, the requirements of GMPs and Lilly Global Quality Standard, and report potential compliance risk in a timely manner through appropriate governance.

主要职能 Key Objectives/Deliverables :

作为偏差管理系统负责人

As Deviation Management System owner role

负责工厂偏差管理规程的维护 ,确保符合礼来质量准则和目标市场的法规要求。 Maintain the site procedure for Deviation Management, to ensure compliance with the requirements from Lilly Quality Standards and Intended markets regulations.

负责 偏差审核会议,并定期对偏差进行趋势分析。Facilitate Review Board, and conduct deviation trend analysis periodically.

作为偏差管理系统的讲师,对工厂员工进行因果关系图、偏差书写技巧等培训。As trainer for deviation management system, provide training of Causal Factor Chart and Deviation Technical Writing, etc for site users.

参加总部会议、与总部业务专家持续沟通及与 其他工厂交流最佳实践, 以支持工厂偏差管理系统的持续改进。Participate in global team conference, continuously improve the deviation management system.

负责维护工厂质量合规相关文件,包括质量手册、场地管理文件、质量体系的管理评审等。

Be responsible for maintaining documentations relevant to the quality compliance, including Site Quality Manual, Site Master File, Management Review of Quality System, etc.

其他与质量相关的事项,如:

To assume other tasks related to QA, such as:

参与偏差调查、变更执行等活动 To take part in deviation investigation, change execution etc.

对其他部门提供改进建议和服务To provide good services and recommendations to other departments for improvement

完成主管 安排 的其他任务

Other jobs assigned by 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 fulfil the work safety responsibilities.

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.

#WeAreLilly

Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
Suzhou, Shanghai, China
Employment type
FULL_TIME

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 139 comparable Associate Quality roles across 49 biopharma companies.

139Comparable roles tracked
130Currently active
49Companies hiring similar roles
23Countries represented

Salary context

30 of 139 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Specialist, Quality Control, Lab Support · Merck $65,100/yr – $102,500/yr
Highest disclosed · Senior Manager, Quality Assurance · Gilead Sciences, Inc. $157,590/yr – $203,940/yr
Peer group range $83,800 – $180,765 (median $161,000)

Where these roles are based

Top locations among the 139 comparable roles

United States57
China15
India14
Ireland11
Japan8
Singapore5

+ 17 more countries

Seniority mix

139 of 139 peers have a known seniority level

Manager116
Associate22
Intern/Fellow/Postdoc1

Therapeutic area mix

0 of 139 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

50%similar
Pfizer Investment Co., Ltd. China Shanghai, China Manager
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Adjacent seniority Same country
50%similar
Sanofi-Aventis Pharma Beijing Co Ltd Beijing, China Manager
Same function Adjacent seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

50%
Supply Operation Quality- Senior Manager
Pfizer Investment Co., Ltd. China · Shanghai, China · Manager
Function Therapeutic area Adjacent seniority Country
50%
IFB-Quality Assurance Manager-QMS
Sanofi-Aventis Pharma Beijing Co Ltd · Beijing, China · Manager
Function Therapeutic area Adjacent seniority Country
50%
M&S-China EM&S Quality Regulatory Manager-Shanghai
Shanghai Rongheng Pharmaceutical Co, Ltd · Shanghai, China · Manager
Function Therapeutic area Adjacent seniority Country
50%
QA Manager Operations
Novartis · Haiyan (Zhejiang Province), China · Manager
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.