Lilly Assoc. QA/QC Consultant, CEM 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 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.
The position will initially be a member of China External Manufacturing, and will function as the primary Quality Contact for providing quality oversight and support for manufacturing activities associated with external partnerships. The support activities related to batch disposition and product testing, validation, Change Management, Deviation Management, Periodic reviews, Auditing, Complaints Management and Document Control.
建立管理外部生产合作伙伴的质量体系Create quality systems to manage external manufacturing partners.
确保外部生产合作伙伴及团队自身运作符合GMP和适合的礼来GQSEnsure GMP and appropriate Lilly GQS compliance for external manufacturing partners and the team’s own operations.
Implement appropriate Lilly Quality Governance to external manufacturing partners to assure successful products launching with required quality.
Participate in business planning to ensure adequate resources are available to support compliance and business needs.
根据需求，参与产品批释放、验证和偏差相关的问题解决和日常决策。Engage in problem-solving and day-to-day decision-making associated with product batch release, validation, and deviations, as needed.
Incorporate Quality by Design concepts where appropriate and strive to continuously reduce deviation, complaints and open quality actions.
与外部生产合作伙伴的质量领导建立良好的合作关系，共同制定决策权的详细认知。Create a strong collaborative working relationship with the external manufacturing partners’ Quality leaders. Jointly develop a detailed understanding of decision-making rights.
Partner with CEM leader to create a strong cohesive team to manage the external manufacturing partners.
Work with global Lilly manufacturing and quality staff to learn best practices that exist elsewhere.
具有五年以上从事药品生产、技术服务和/或质量管理的GMP相关经验5+ years GMP experience including roles associated with production support, TS/MS and/or Quality
本科学历（化学、生物、生命科学、制药或工程相关专业优先）Bachelors or equivalent (Chemistry, Biology, Life Sciences, Pharmacy or Engineering related degree preferred).
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 ( LillyRecruitingCompliance@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.
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!