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Be part of something altogether life-changing! Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies. At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40+ countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term. Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics. The Manufacturing Science and Technology (MSAT) Scientist II for Cytiva is responsible for providing technical pre and post-sale support for the integration of Cytiva filtration technologies into customer process in collaboration with the commercial team and R&D. This position is part of the EU Filtration Customer Success (FCS) team and will be fully remote.
Job Responsibility
Application of Cytiva Bioprocess filtration products (normal and tangential flow filtration) to create process solutions
Conduct feasibility assessments, technical consultations, training and bench trials at customers
Technical consultation involving scale up/scale down testing plans and data review, sizing and compatibility recommendations, troubleshooting customer technical issues and field investigations
Maintain an up-to-date knowledge of current regulatory trends, issues and guidelines relating to the products being supported
Requirements
Bachelor’s Degree in a relevant field
3+ years of experience in the Biopharmaceutical industry, preferably in MSAT or PD role
Technical support experience
Fluent English and good communication skills
Valid driving licence
Willing and able to travel up to 50%, primarily within Europe
Nice to have
Master’s Degree in life science, Chemical or Biological Engineering
Advanced proficiency in German
Knowledge of the regulatory framework for drug manufacturing
Knowledge of main purification techniques used for drug manufacturing