Associate-QA Compliance
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
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.
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.
Where these roles are based
Top locations among the 139 comparable roles
+ 17 more countries
Seniority mix
139 of 139 peers have a known seniority level
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.
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.
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.