Help us improve access to life-changing therapies that can transform human health

We are Cytiva, a global provider of technologies and services that advance and accelerate the development and manufacture of therapeutics. Formerly part of GE Healthcare, we have a rich heritage tracing back hundreds of years, and a fresh beginning since 2020.

Our customers undertake life-saving activities. These range from fundamental biological research to developing innovative vaccines, biologic drugs, and novel cell and gene therapies. Our job is to supply the tools and services - the pots, pans, soups and sauces - they need to work better, faster and safer, leading to better patient outcomes.

What you’ll do

• Responsible for QA document control and site quality training, handling Cytiva learning system;
• Support and assist QA team to deliver internal/external audit/ NC workflow /CAPA procedure/ change control management etc.;
• Support manufacture and CHU team to handling the internal quality issues and customer complaint;
• The others work arranged by QA manager.

Who you are

• Be familiar with manufacture enterprise process and bachelor's degree or above in manufacturing related majors.
• Have 2~3 years' experience of quality assurance and quality management system.
• Familiar with ISO9001/ISO13485 system and other medical device related quality system requirements.
• Be familiar with office software such like Word/Excel/PPT and so on.
• CET-4 and above, have good English communication skills
• Have the experience with continuous improvement, familiar with CAPA process, and proficient in quality improvement tools such as QC 7 tools and lean six sigma.
• Have strong judgment, organizational coordination, communication skills and strong sense of responsibility.

Who we are

Cytiva is a 3.3 billion USD global life sciences leader with nearly 7000 associates across 40 countries who are dedicated to our mission to advance and accelerate therapeutics. As a trusted partner to customers that range in scale and scope, Cytiva brings efficiencies to research and manufacturing workflows, ensuring the development, manufacture and delivery of transformative medicines to patients.

Cytiva is part of the Danaher family of companies, a global science and technology innovator committed to helping customers solve complex challenges and improving quality of life around the world.

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

For more information, visit www.danaher.com.