Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Cytiva, one of Danaher’s 15 operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life. 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. Take your next step to an altogether life-changing career. Learn about the Danaher Business System which makes everything possible. In this role, you will have the opportunity to: Drive innovation through scientific analysis and review of current thinking/state of the art in the medical water market. Lead initiatives to identify future market drivers and applications through scientific research and development of relationships with Key Opinion Leaders, industry bodies and government organizations. Lead clinical evaluation and design validation within Pall Medical to ensure products meet design and end-user requirements in medical water applications. Develop and deliver technical applications and scientific training and expertise to connect medical water applications with product performance requirements to internal and external stakeholders across Pall Medical product portfolios globally. Author scientific papers, technical position pieces, abstracts, posters and blogs and present at conferences, seminars and webinars. The essential requirements of the job include: PhD in a relevant subject and significant experience in technical applications support in a clinical environment. Ability to translate understanding of the business, markets, guidelines and regulatory landscape to inform strategic direction of the Medical Business. Track record in relationship building with diversity of internal and external stakeholders/key opinion leaders and ability to anticipate potential points of conflict and drive to consensus. It would be a plus if you also possess previous experience in: Leading cross functional projects and remote teams. Understanding of global regulatory medical device requirements for new product introduction. Conducting in-clinic product performance studies in compliance with applicable regulations and guidelines. Join our winning team today. Together, we’ll 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. For more information, visit www.danaher.com .