工艺工程师

Work Your Magic with us!

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US. 

Your role:

Job Objective：
Be responsible for assembly process daily management with focus on each zone failure rate analysis, set issue improvement plan and lead team to implement that.
Define the standard/requirement of single use product manual assembly.
Have capability on preparing related validation plan and project (for equipment/product/clean room),and be indecently complete the validation complete the validation report .

Main Responsibilities：
Be responsible for assembly process daily management with focus on each zone failure rate analysis, set issue improvement plan and lead team to implement that.
Define the standard/requirement of single use product manual assembly.
Monitor process quality issue once received customer complaint or internal quality issue from QA, will lead team to do investigation, root cause analysis and find action plan, follow up till closed;
Have capability on preparing related validation plan and project (for equipment/product/clean room), and be indecently complete the validation complete the validation report;
Support/Carry out outsource sterilization possibility study and final validation;
Be responsible for area SOP, have capability to train other team members;
Comply with the company's safety and quality regulations and participate in the safety and quality training organized by the company 遵守公司安全和质量相关规定，参加公司组织的安全和质量培训
Other duties required by the superior

Who you are:

Qualification Requirement:
University degree 
5 years+ experience of pharmaceutical/life science/Medical device   experience , GMP is a plus 
Good skills with MS office software
Service mindset and good communication skills
With English skills 
Good teamwork attitude, initiative and hardworking, good communication skills.

HR: 958989
Functional Area: Manufacturing

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!
 
Apply now and become a part of our diverse team!

If you would like to know more about what diversity, equity, and inclusion means to us, please visit https://www.emdgroup.com/en/company/press-positions.html