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Bring more to life

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, 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.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year. From uncovering the next clinical breakthrough, to rapid and reliable sample analysis, to more rigorous decision making—we are enabling clinicians to deliver the best possible care to their patients with improved efficiency, clinical confidence, adaptive collaboration, and accelerated intelligence.

Learn about the Danaher Business System which makes everything possible.

On the Supplier Quality Coordinator position you will report to the Regional Manager – Channel Partner Management Supplier Quality & Regulatory. The Specialist role is responsible for Supplier and Third Party Products to support regional commercial operations.

In this role, you will have the opportunity to:

• Lead and execute Third-Party Products IVDR transition follow-up activities, collaborating closely with suppliers to ensure readiness, compliance, and a robust post-transition supply chain.
• Maintain, implement, and continuously enhance Supplier Quality Management System (QMS) processes and infrastructure to ensure best-in-class compliance and strong business support for the commercial organization in EMEAI.
• Manage supplier lifecycle activities — including approval, inactivation, and maintenance — ensuring full data integrity and adherence to internal and external regulatory requirements.
• Support and lead supplier remediation projects, providing expert guidance and strategic solutions to mitigate risks and ensure compliance.
• Drive departmental objectives, report progress, and influence stakeholders across functions to achieve business success.

The essential requirements of the job include:

• University Degree in Science or a related technical discipline.
• Experience in Supplier Quality or Regulatory Affairs within the Medical Device or Pharmaceutical industry is an advantage
• Understanding of IVDR and experience operating within a commercial medical device environment.
• Excellent cross-cultural communication and collaboration skills, with the ability to work effectively across regions and teams.
• Fluent in English (both written and spoken).
• Strong IT literacy, including proficiency in Microsoft Office and experience using QMS software.
• Travel, Motor Vehicle Record & Physical/Environment Requirements, Ability to travel for up to 10%.

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

• Experience working across multiple geographies and within matrixed organizations is welcomed
• Familiarity with Regulatory Affairs (IVD/Medical Devices) and supplier quality frameworks would be plus
• 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.
• We are opened also for a student biomedical type of a faculty who can offer min 30hrs a week

For more information, visit www.danaher.com