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 Application Specialist at Cytiva is responsible for providing biopharma downstream process support, knowledge, and trainings to cross-functional teams and customers.

This position is part of the Customized Bioprocess Solutions located in Uppsala and will be hybrid. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

In this role, you will have the opportunity to:

• Establish functional and application requirements both on hardware and software for customized bioprocess equipment.
• Plan, lead and test functionality of bioprocess applications.
• Provide application/process support and training to cross-functional teams and customers during sales, projects, and post-sales activities.
• Secure development and Intellectual Property of bioprocess process technologies and offerings.
• Use market and product knowledge to assist cross-functional team in developing process understanding, translating customer process needs into technical requirements.

The essential requirements of the job include:

• M. Sc./BSc or above in Biotechnology or Life Sciences.
• Several years of relevant experience in Life Sciences or Biopharma industry.
• Demonstrated knowledge of bioprocessing and the manufacturing process of biopharma products.
• Demonstrated understanding of cross-functional needs and interdependencies to successfully deliver a superior customer experience.
• Understanding of cGMP regulatory environment.

It would be a plus if you also possess previous experience in:

• Public speaking and lecture experience desired.
• Understanding and engaging in technical discussions of complex material to make it understandable.
• Managing and resolving conflicts, communicate issues, and propose responsive solutions to both internal team members and external customers in a global setting.

At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, hybrid working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a hybrid work arrangement in which you can work part-time at the Company location identified above and part-time remotely from your home. Additional information about this hybrid work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.