Lead Scientist

Danaher Corporation

Lead Scientist at Cytiva focusing on downstream process development for biomanufacturing projects. Collaborating with customers and providing expert guidance in a research-driven environment.

Posted 7/9/2026full-timeIncheon • 🇰🇷 South KoreaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in purification process development for monoclonal antibodies, recombinant proteins, and vaccines, with a strong understanding of GMP manufacturing and FDA/EMEA regulations. Capable of designing and delivering training in biomanufacturing while fostering collaborative relationships with customers and internal teams.

Highest-signal resume keywords

Purification Process DevelopmentGMP ManufacturingFDA/EMEA RegulationsBiomanufacturing Training DevelopmentContinuous Improvement in Bioprocessing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Purification Process DevelopmentBiomanufacturingScale-Up PrinciplesValidation KnowledgeSingle-Use SystemsHybrid SetupsTraditional SetupsCMC DocumentationProcess EnhancementBiological Processing

Soft Skills

Excellent CommunicationCollaborative WorkCustomer Focus

Industry Keywords

Monoclonal AntibodyRecombinant ProteinVaccinesMRNABiologicsDownstream Process DevelopmentFast TrakR&D OrganizationsMatrixed EnvironmentContinuous Improvement

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

5+ year of relevant experience with purification process development of monoclonal antibody, recombinant protein, vaccines or mRNA 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
Excellent communicator with English language proficiency, with demonstrated ability to work in a collaborative, matrixed, and customer focused environment.

Benefits

Comp & perks

Comprehensive, competitive benefit programs
Health care program
Paid time off