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 Associate Senior Project Manager (m/f/d) for Cytiva is responsible for the execution of technical projects supporting current and future business growth. The projects focus on multiple products for the Cell Therapy business. The project manager has a key leadership role not only with the technical team but across all functions and customers to achieve a successful outcome whilst using Danaher Business Tools and robust project and team management methods. The ideal candidate will have a proven track record in managing and delivering projects on time and within budget, while ensuring compliance with organizational standards and quality management systems.

This position reports to the Sr. Manager, Project Management and is part of the Cell Therapy R&D Department located in Grens, Switzerland and will be an on-site role.

What you will do:

• Work closely with Strategic Marketing, Product Management, and R&D to understand market and customer needs, and help define product requirements

• Enable collaborative definition of project scope, goals, deliverables, schedules, resource allocation, and cost estimate for new product development and sustaining projects

• Lead cross-functional teams to effectively deliver projects on time and within budget, evaluating and managing project risks and issues, leveraging the appropriate resources within and/or outside the department

• Work closely with clients, suppliers, and internal teams across different locations to proactively anticipate challenges, coordinate project timelines, and facilitate decision making

• Communicate across functional departments, and provide periodic stakeholder and steering committee communications, and escalate concerns and issues as necessary

• Maintain organizational standards of performance, while ensuring compliance with QMS requirements, product lifecycle process, Finance, Legal, Sourcing, EHS, and other functional support processes

• Identify and share best practices of application of tools and ways of working to drive continuous improvements

Who you are:

• Bachelor’s degree in engineering discipline (mechanical, electrical, software, systems, industrial, biomedical, or related discipline) and 5+ years project leadership/management experience within product development, manufacturing or research environment, preferably in the healthcare industry or other highly regulated industry

• Demonstrated ability to lead and motivate cross-functional teams, and drive projects to completion on time and within budget, while satisfying quality and performance requirements

• Proficient in project management principles (e.g., planning, resource allocation, cost estimation, risk analysis, communication) and tools. Professional Project Management certification is an asset (e.g. PMI). Experience of end-to-end project management within product lifecycle process

• Demonstrated ability to manage stakeholders in a matrix organization and to collaborate with diverse and global cross-functional teams. Demonstrated experience of working closely with clients and suppliers to deliver results. Demonstrated ability to work with decision makers.

• Demonstrated negotiation and conflict resolution skills. Demonstrated analytical and problem-solving skills. Ability to work in a dynamic and fast pace environment. Strong verbal and written communication skills. Fluent in English and preferably also French.

• Familiarity and experience of FDA, ISO regulations and standards

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

• Danaher Business System (DBS) Tools

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – for up to 10% travel (overnight, within EU and USA)

• Must have a valid driver’s license with an acceptable driving record

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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