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
1.Lead downstream pilot scale project to manufacture protein for pre-clinical study. Support to prepare IND-filling document.
2.Develop expertise on downstream process development, operation of large-scale bioprocess equipment and CFDA regulations.
3.Conduct purification process development project for customer and deliver study reports to customer. Support customer to accelerate their new drug development progress from lab scale process to large scale production.
planning and implementing training events. Deliver lectures and lab hands-on work.
5.Understand marketing trends to support sales department and customers with expert advice. Work closely with field application specialists and support customers by offering trouble-shootings, bioprocess development services and consulting.
Offer on-site support to customers for approximately up to 20% of the working time.
6.Support GE downstream product in maintaining scientific leadership by designing and delivering creative solutions to customer’s manufacturing challenges.
Add value to Cytiva’s customers by identifying continuous improvement opportunities in their bio-manufacturing processes.
Who you are?
1.Master or PhD of chemical-engineer or biochemist or drug science related with >
3 years or bachelor with >
3 years of industrial experience in process development or production of biopharmaceuticals.
2.Industrial experience and theoretical knowledge of the basic techniques used for downstream purification of biopharmaceuticals (filtration, chromatography, centrifugation, etc.
at pilot or commercial production scale. Good understanding of the basics of process economy.
3.Good project management experience and work with global team.
4.Accomplished presenter to critical audiences or teacher.
5.Good people skills. Proven ability to work in team environment and able to develop working relationship with customer.
6.Experience on preparing IND and NDA documents.
7.Socially competent to handle sensitive customer relationships, demonstrated problem-solving skills.
8.Demonstrated ability to deliver results while working on multiple project simultaneously, in a cross-functional team and in an international environment.
9.Excellent written and spoken skills in English and Chinese.
Who we are?
Whatever your role, we bring purpose and challenge into our everyday work. If you are driven to make the world a better place thanks to science and medicine, you’ll feel right at home here.
If you’re flexible, curious and relentless, you’ll belong. If you are excited about a global culture, this can be the place to further your career.