Senior Process Engineering

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Supply Chain Engineering

Job Sub Function:

Process Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Xian, Shaanxi, China

Job Description:

1. 在有限的指导下负责和协调辅料/APIs/包材物料供应商切换项目、工艺改进项目以及新技术引入项目等，包含以下主要活动：Leads and coordinates projects for Source change of Excipients/APIs/Packaging materials; Process improvements and the introduction of new technology under supervision including as needed：

a.     组建核心团队，根据FPX启动并管理项目时间表；Setting up the core team, kicking off the project along the FPX procedures and manages project timeline;

b.      追踪核心团队成员完成可交付的成果；Follow up core team members to achieve deliverables;

c.      通过完成项目的里程碑以及重要事项，实现项目的目标；Realize the project outcomes through the project milestones and deliverables;

d.      充分认识核心技术，使其能够适宜运用到工厂的设备上；Fully understands the core technology, and adapts it to the site equipment and suitability

e.      完成技术转移，包括试验批、验证批和报告；Completes the technical transfer, including development batches, validation batches and reports;

2. 独立有效地推进相关的验证工作，包括工艺验证、包装验证和清洁验证。能够草拟验证草案和报告；Drives related validations independently and efficiently that including process validation, packaging validation and cleaning validation. Be capable to design validation protocol and report;

3. 完成工厂不符合事件的调查，通过使用科学的解决方案和六西格玛方法来确定并证实问题的根本原因；Completes investigations for site process non-conformances by using scientific problem solving and six sigma techniques to determine and then prove the root cause;

4. 积极主动的提出工厂工艺改进的建议，以提高工艺的粗放度进而减少不符合事件的发生；Proposes opportunities of improvement the processes on site to proactively improve the process robustness and reduce non- conformances;

5. 能与重要的利益相关方进行有效沟通，并加快解决业务合作伙伴复杂的问题。Efficiently communicates within stakeholders and facilitates resolution of less complex business partner issues.

6. 确保cGMP，财务以及其他法规的完全合规。Ensures full compliance to cGMP, Finance and other regulations.

 

 

Required Skills:

 

 

Preferred Skills:

Analytical Reasoning, Computerized Equipment Skills, Emerging Technologies, Gemba Kaizen, Issue Escalation, Lean Supply Chain Management, Problem Solving, Process Control, Process Engineering, Process Oriented, Product Improvements, Science, Technology, Engineering, and Math (STEM) Application, Situational Awareness, Supply Planning, Technical Research, Technologically Savvy, Validation Testing