Vacant job

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 Supplier Quality Operations Program Manager for Cytiva is responsible for managing global process and system initiatives across Cytiva Supplier Quality.

This position is part of Supplier Quality located in Uppsala, Sweden and will be on site. At Cytiva, our vision is to advance future therapeutics from discovery to delivery.

What you will do:

• Lead global programs across Cytiva Supplier Quality with focus on supplier qualification, auditing, CAPA/RCA, change notice management, data analytics & QMS training
• Lead operations management activities within Cytiva Supplier Quality
• Work directly with cross-functional peers to implement or refine input, control and output streams of cross-functional processes
• Identify opportunities for continuous improvement of supplier quality process and operations

Who you are:

• Bachelor’s degree in Engineering or technical field; a quality professional with a minimum of 5 years of quality related work experience.
• Experience in the biotechnology and/or pharmaceutical industry, preferably both.
• Possess strong data analysis skills and problem-solving abilities, collaborate with teams and deliver impact.
• Knowledge of supplier quality management workstreams including qualification, auditing, change management, CAPA/RCA, QMS development and training program development.
• Valid Swedish work permit

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel – 15% travel, overnight, global
• Must have a valid driver’s license with an acceptable driving record

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

• Veeva, SFCD, QlikSense, Smartsheet, Excel software experience
• Demonstrated commitment to DBS Fundamentals, holding a CP or ACP in VSM, TPI, PSP, and Daily Management