Sr Engineer, Product Lifecycle
Job Summary
What if the work you did every day could impact the lives of people you know Or all of humanity
At Illumina we are expanding access to genomic technology to realize health equity for billions of people around the world. Our efforts enable life-changing discoveries that are transforming human health through the early detection and diagnosis of diseases and new treatment options for patients.
Working at Illumina means being part of something bigger than yourself. Every person in every role has the opportunity to make a difference. Surrounded by extraordinary people inspiring leaders and world changing projects you will do more and become more than you ever thought possible.
Position Summary:
Act as primary point of contact for OEM partners during on-market partnership program and involve in NPI partnership program for relevant platform. Drive and meet project deliverables and collaborate with various cross functional teams for on-market support and engineering changes that affect partners to ensure smooth acceptance and implementation in process testing and production. Support other GC GO projects as needed.
Position Responsibilities:
- Act as primary point of contact for OEM partners during on-market partnership program for fulfilling OEM partners deliverables.
- Collaborate with CN MFG SG MFG and CN S&S team stakeholders to drive the planning and execution of engineering changes and platform roadmaps that can affect partnerships configuration and registration.
- Participate actively and able to facilitate troubleshooting problem solving failure analysis root cause and corrective action processes as required.
- Drive project management includes creation and maintenance of detailed project plans and schedules for team members providing status reports and making presentations to stakeholders.
- Carry out documentation responsibilities include but not limited to driving generation of detailed engineering drawings Bill of Materials test reports assembly procedures and design validation plans.
- Support partnership documentation filing and submission.
- Regular travel to partners manufacturing sites to keep consistent communication is anticipated.
- Support other team tasks assigned by the managere.g. stakeholder coordination meeting/workshop facilitation action item tracking report generation training program executionto ensure timely team delivery and quality.
- Other tasks assigned by manager.
Listed responsibilities are an essential but not exhaustive list of the usual duties associated with the position. Changes to individual responsibilities may occur due to business needs.
Position Requirements:
- Knowledge of manufacturing process hands-on exposure to Product Lifecyle Management (PLM)/Teamcenter workflows (CN/CR) and ability to drive documentation change-control and closure.
- Be able to effectively coordinate and facilitate cross-functional teams interface well with the manufacturing quality regulatory supply chain and service organization and has a proven track record of transferring products to manufacturing.
- Strong organizational skills attention to detail and accuracy and the ability to work independently in a team environment are essential.
- Self-disciplined and good prioritization skills; able to assess urgency and importance and manage multi-tasking and urgent scenarios effectively to meet deadlines.
- Effective and strong communication skills - both written and verbal. Able to articulate and discuss ideas and persuade others to achieve common outcomes.
- Proficiency with project and collaboration tools.
All listed requirements are deemed as essential functions to this position; however business conditions may require reasonable accommodation for additional tasks and responsibilities.
Preferred Experience/Education/Skills:
- Typically requires a minimum of 2 years of related experience with a bachelors degree or above in Life Sciences / Engineering / Business required; PMP certification preferred.
- Experience with FDA and NMPA regulated medical device product development preferred.
- Fluency in English and Mandarin desired.
如果每天的工作能够影响你所认识的人抑或全人类的生活你将会作何感想
在因美纳我们正在扩大基因组技术的使用范围为全世界数十亿人实现健康公平我们的努力促成了变革生活的各项发现通过对疾病的早期检测和诊断以及为患者提供新的治疗方案这些发现改变了人类健康
在因美纳工作意味着不断突破自身实现更高价值每个人在每个职位都有机会做出改变在卓越不凡的同僚鼓舞人心的领导和改变世界的项目的包围中你将奋发进取你的改变将超乎你的想象
岗位概述
在产品已上市阶段on-market作为 OEM 合作伙伴的主要对接人负责相关合作项目的日常协调同时参与相关平台的新产品导入NPI合作项目协同各相关跨职能团队推动并落实项目交付要求支持产品上市后的运营及工程变更确保涉及 OEM 合作伙伴的流程测试及生产能够顺利接受并实施根据业务需要支持其他大中华区GO 相关项目
岗位职责
- 在产品已上市阶段on-market作为 OEM 合作伙伴的主要对接人协调并推进相关合作事项确保 OEM 伙伴交付要求的落实
- 与中国制造CN MFG新加坡制造SG MFG及中国服务与支持CN S&S等相关团队协作支持受工程变更和平台路线图影响的合作配置与注册工作的规划与执行
- 根据需要积极参与并协助推进故障排查问题解决失效分析根因分析及纠正措施相关流程
- 支持项目管理相关工作包括制定并维护项目计划和进度安排向相关方提供项目状态更新并进行必要的汇报与沟通
- 承担相关文档工作包括但不限于推动工程图纸物料清单BOM测试报告装配流程及设计验证计划等文件的准备与完善
- 支持 OEM 合作相关文件的整理归档及提交工作
- 根据业务需要需定期前往 OEM 合作伙伴的制造现场以保持持续有效的沟通
- 支持经理分配的其他团队工作例如相关方协调会议或工作坊组织行动项跟踪报告准备及培训项目执行等确保团队按时高质量交付
- 完成经理分配的其他相关工作
以上所列的任务和职责是本岗位的基本职能工作开展中可能需要合理完成额外的任务和职责
岗位要求
- 具备制造流程相关知识熟悉产品生命周期管理PLM/TeamcenterCN/CR流程并能够推动文档变更控制及闭环管理
- 能够有效协调和促进跨职能团队合作与制造质量法规供应链及服务等相关部门保持良好的工作接口并具备产品从研发阶段成功转入制造阶段的实际经验
- 具备较强的组织能力注重细节和准确性能够在团队环境中独立开展工作
- 自我管理能力强具备良好的任务优先级判断能力能够在多任务及紧急情况下合理安排工作确保按期完成目标
- 具备良好的沟通能力包括书面和口头表达能够清晰阐述观点与相关方有效讨论并推动达成共识
- 熟练使用项目管理及协作类工具
所列要求为本工作岗位的基本职能在不同的业务情况下可能会做出合理增加任务和职责的调整
期望的工作经验/教育背景/技能
- 本科及以上学历生命科学工程或商科相关专业优先通常需具备 2 年及以上相关工作经验持有 PMP 认证者优先
- 有 FDA 和 / 或 NMPA 监管环境下医疗器械产品开发或制造相关经验者优先
- 具备良好的中英文沟通能力者优先
We are a company deeply rooted in belonging promoting an inclusive environment where employees feel valued and empowered to contribute to our mission. Built on a strong foundation Illumina has always prioritized openness collaboration and seeking alternative perspectives to propel innovation in genomics. We are proud to confirm a zero-net gap in pay regardless of gender ethnicity or race. We also have several Employee Resource Groups (ERG) that deliver career development experiences increase cultural awareness and offer opportunities to engage in social responsibility. We are proud to be an equal opportunity employer committed to providing employment opportunity regardless of sex race creed color gender religion marital status domestic partner status age national origin or ancestry physical or mental disability medical condition sexual orientation pregnancy military or veteran status citizenship status and genetic information. Illumina conducts background checks on applicants for whom a conditional offer of employment has been made. Qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable local state and federal laws. Background check results may potentially result in the withdrawal of a conditional offer of employment. The background check process and any decisions made as a result shall be made in accordance with all applicable local state and federal laws. Illumina prohibits the use of generative artificial intelligence (AI) in the application and interview process. If you require accommodation to complete the application or interview process please contact To learn more visit: The position will be posted until a final candidate is selected or the requisition has a sufficient number of qualified applicants. This role is not eligible for visa sponsorship.
Required Experience:
Senior IC