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

We are seeking an Associate Scientist to lead downstream process development and training activities at the APAC Fast Trak Center located in the Songdo area of Incheon, Korea.

• Conduct downstream process development on customer projects, and maintain and operate small- and large-scale bioprocess equipment
• Maintain accurate and complete records of all work, and report to customers and management in oral and written manner
• Design, develop and deliver training courses, theoretical as well as practical, in the field of biomanufacturing for both internal and external customers
• Work with, and provide expert advice to, customers in a strongly collaborative environment
• Add value to Cytiva’s customers by identifying continuous improvement opportunities in their bio-manufacturing processes and designing and implementing innovative process enhancement
• Develop and maintain relationships with the regional commercial and marketing teams, as well as the global Fast Trak and R&D organizations

Who you are

• Experience with purification process development of monoclonal antibody, recombinant protein, or vaccines in an industry setting
• Understanding of principles and theory behind unit operations for processing biologicals with knowledge in principles of scale-up, validation, single-use, hybrid and traditional set ups
• Experience in GMP manufacturing and working knowledge of FDA/EMEA regulations for biologics including experience in CMC documentation preferred
• Conversational level English language proficiency, with demonstrated ability to work in a collaborative, matrixed, and customer focused environment
• Earned a Bachelor’s degree in Life Sciences, Chemical Engineering or related Life Sciences field; advanced degree preferred

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.

Want to know more? Experience life at Cytiva on our Careers website, Instagram channel and LinkedIn page!

Cytiva is global life sciences leader with over 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.

Danaher Corporation and all Danaher Companies are equal opportunity employers that evaluate qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. The “EEO is the Law” poster is available here