Danaher Jobs

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.

As a Product Scientist within the CTO Genomic Medicine organization organization at Cytiva, you will be an integral member of a passionate team at the forefront of automating biological cell processing.

You will be responsible for managing the technical compliance of the cryopreservation product portfolio in strong collaboration with cross-functional stakeholders and in this role you will be leading various activities such as investigating customer complaints, performing root cause investigation, identifying corrective and preventive actions working with multidisciplinary teams and customers, performing verification and validation activities and performing trending analysis and reporting.

What you’ll do

• Participate and represent R&D in the complaint handling investigation team, perform investigations, data analysis and experimental tests to identify root causes. Evaluate findings to formulate corrective action plan.

• Collaborate and coordinate with a multidisciplinary R&D team to evaluate and resolve engineering and quality-related problems.

• Take the lead to translate between the parties to facilitate customer support and quality-related problems resolution, in close R&D collaboration with the engineering and biological team matter experts.

• Build working relationships with the customer support teams, field engineer and field application specialist teams and end-users (biotech or Pharma companies) and increase product knowledge across the customer facing teams.

• Master processes and tools and take the lead on process/tools/document optimization to improve the overall change control and CAPA process efficiency in compliance with ISO9001 standards and other QMS requirements.

• Regular reporting on customer feedback, CAPA trending and progress enabling product evolution.

• Write technical documentation including root cause investigation, test plan and report, and user technical documentation for a wide range of target audience.

• Assist with internal and external Quality audits and participate to market support programs.

• Deliver on-time, communicate effectively, and resolve conflicts, encourage constructive dialogue within the cross-functional teams.

• Acquire DBS knowledge and practice DBS processes.

  Who you are

• Bachelor’s or Master’s Degree in physics, engineering, or life science with 6 years of relevant experience in the Life Sciences or medical sector or Ph.D. with 2 years of relevant experience.

• Experience working with complex product in a multidisciplinary environment, ideally involving broad hardware, software, and single-use technologies.

• Good theoretical know-how in understanding engineering disciplines and good understanding of human cell biology.

• Statistical methods and tools for performing qualitative and quantitative data analysis with demonstrated ability to investigate and troubleshoot, strong critical thinking, analytical and problem-solving skills, and attention to detail.

• Demonstrated ability to clearly communicate (oral, written) across global, cross-cultural, cross-functional teams and stakeholders.

• Customer-oriented mindset, autonomous at work, good organizational skills, creative, and comfortable with change.

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

• Cell cryopreservation methods, especially in the context of immunology.

• Knowledge and practical experience of relevant regulations (ISO 9001, cGMP), specifically for the US and European market.

• Fluent in English, a second language is a plus.

At Danaher we bring together science, technology and operational capabilities to accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life. Our global teams are pioneering what’s next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit www.danaher.com.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.