Sales Specialist, Validation Services (m/w/d)

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 matt. And 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 activities undertake life-saving 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 altogether life-chan career. Learn about the Danaher Business System which makes everything possible. As a key contributor within Cytiva, the Sales Specialist, Validation Services DACH region plays a pivotal role in driving the growth and strategic positioning of our Validation Services solutions within the Fast Trak portfolio. This highly independent and impactful position developing and executing a comprehensive sales action plan aimed at achieving and surpassing European sales targets, while welcoming Cytiva's leadership in the biopharma services market. This position is part of the PDVS commercial organization. It reports to the Senior Director Global Sales, PDVS. Assigned territory is Germany, Austria and Switzerland. It will be fully remote and can be located anywhere in the assigned region. At Cytiva, our vision is, to advance therapeutics from discovery to delivery. Develop and execute a sales action plan for the assigned region to meet or exceed, quarterly, and annual sales and orders through direct sales and partnership with commercial colleagues Establish relationships with customer end-users and leaders in the assigned region to successfully promote Cytiva filter validation services solutions, technologies and capabilities. Customer environment is the biopharma and CDMO space targeting molecules in pre-clinical and clinical phase. Involving into regulatory discussions with customers will be key. Provide consultative technical support for processes that require filter validation services and develop and support commercial solutions that meet or exceed the customers' expectations. Report and communicate all business opportunities, solution concepts and strategies while participating and leading funnel review calls. Effectively utilize Funnel Management. Expand the filter validation services business by gaining market share by establishing strong relationships with end-users and successfully promoting Cytiva filter validation services capabilities. 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. 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.

Educational Background: BSc in Biotechnology/Chemical Engineering/Life Sciences or equivalent experience. Industry Experience: Strong experience in bioprocess/pharmaceutical manufacturing/CDMO environment or related field Commercial Acumen: First sales experience in the Pharmaceutical, Biotech or CDMO field is preferred but not mandatory. Commercial training program will be provided. Technical Understanding: Strong understanding of regulatory and analytical aspects in the validation environment Travel, Motor Vehicle Record & Physical/Environment Requirements: Ability to travel – up to 30% with incl. occational overnight, within region as well as occasional overseas travels Must have a valid driver's license with an acceptable driving record It would be a plus if you had previous experience in: Experience in validation services for complex molecules search as mAbs as well as new modalities search as viral vectors, mRNA, pDNA, etc. and new modalities to identify opportunities for further growth At Cytiva we believe in designing a better, more sustainable workforce. We recognize the benefits of flexible, remote working arrangements for eligible roles and are committed to providing enriching careers, no matter the work arrangement. This position is eligible for a remote work arrangement in which you can work remotely from your home. additional information about this remote work arrangement will be provided by your interview team. Explore the flexibility and challenge that working for Cytiva can provide.

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