Application V&V Engineer (m/f/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 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.

The Application V&V Engineer (m/f/d) is responsible for Verification and Validation of Application interfacing with other subsystems (plan, procedures, tests execution) in compliance with system and sub-system requirements to meet relevant regulatory standards, customers' expectations and to the highest QMS quality standards.

This position reports to the System V&V Manager and is part of the System Verification & Validation team located in Signy and will be an on-site role.

What you will do:

• Collaborate closely with System Engineering, System V&V lead, Application, Software, Product Managers, Project Managers and Product Engineering to ensure all relevant system interfaces are considered and that the system functions effectively as a whole.

• Participate in the development of roadmaps, plans and priorities. When needed, participate in Applications team Scrum meetings (sprint planning, retro, stand-ups).

• Collaborate and contribute to V&V deliverables of the Applications sub-system (scope, strategy, plans, procedures, methods, tests, traceability matrices and reports) while acting as a technical mentor for Application V&V engineers, fostering skill development and consistent application of V&V standards.

• Collaborate and contribute to Applications sub-system risk analysis deliverables, traceability of risks of Applications sub-system and system interfaces.

• Subject matter expert in verification and validation activities, sampling methods and risk analyses

• Support failure investigations related to defects at the interface between System and Applications sub-system in collaboration with V&V Engineers, System Engineering, Project Managers, Product Engineering. Address and define way forward when gaps are identified in requirements, procedures, methods pertaining to development and V&V.

• Actively support and contribute to continuous improvement of system V&V activities by optimizing processes, tools, and methodologies

Who you are:

• Master’s degree in Systems Engineering, Computer Engineering, Life Sciences, Biomedical Engineering, or a related field.

• Minimum 10 years of successful experience in new product development, product care, project management and manufacturing science and technology, ideally for the medical or life science industry involving cross-functional teams.

• Demonstrated experience in defining and managing verification and validation plan and execution.

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

• Fluent in English, second language a plus.

• Result driven, autonomous at work, dynamic, creative, initiatives welcomed.

• Proficiency in programming languages such as Java, Python, or C#.

• Strong analytical skills and structured approach to problem-solving.

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

• Software development lifecycle (requirements, design, implementation, testing, maintenance)

• Product lifecycle and relevant know-how about regulations such as ISO 9001, ISO13485, cGMP, specifically for the US and European market.

Cytiva, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

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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.