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.

The Global Supplier Quality Engineer - Systems and Innovation for Beckman Coulter Diagnostics is responsible for l eading the development of best-in-class supplier quality processes, tools, and system s, with emphasis on PPAP, APQP, and the integration of automation to drive improvements throughout our global supply base .

This position reports to the Sr. Director of Global Supplier Quality responsible for glob al supplier quality strategy and is part of the Global Supplier Quality team. The job location for this role is in-person, preferably, Chaska MN, Miami FL or Brea CA.

In this role, you will have the opportunity to:

• Design and Implement Scalable Quality Systems Develop and deploy supplier quality processes, digital tools, and intelligent workflows that incorporate best practices in APQP, PPAP, FMEA, Control Plans, and validation to drive global standardization and process efficiency

• Enable Data-Driven Decision-Making Build dashboards, automation, and real-time analytics to enhance visibility, support proactive quality planning, and drive continuous improvement across the global supply base.

• Provide Strategic Guidance and SME Support ​Act as a subject matter expert to global and site-level SQE teams, offering leadership on supplier quality planning, digital integration, and advanced quality tool utilization.

• Lead Cross-Functional and Transformational Initiatives Drive projects focused on supplier readiness, onboarding, and long-term capability development, emphasizing scalability, lean principles, and digital transformation. Utilize application of DBS tools and kaizen methodologies to identify and implement opportunities for innovation, process simplification, and global standardization.

• Collaborate and Cultivate Partnerships for Performance Improvement Work closely with cross-functional teams and external partners to embed smart quality systems throughout the product lifecycle and deliver sustained improvements in quality, delivery, cost, and compliance.

The essential requirements of the job include:

• Bachelor’s degree in technical field with 9 + years experience or Master’s degree in field with 7 + years experience or comparable

• 5 + years of experience in supplier quality, advanced quality planning, or quality systems engineering.

• Demonstrated expertise in APQP, PPAP, FMEA, MSA, SPC, and related quality tools within regulated manufacturing environments.

• Experience working with or implementing digital tools, AI platforms, or automated quality systems is strongly preferred.

• Strong project leadership, analytical, and communication skill s.

Travel, Motor Vehicle Record & Physical/Environment Requirements:

• Ability to travel - Up to 15% globally based on business need

It would be a plus if you also possess :

• Experience in FDA-regulated or medical device manufacturing environments.

• Familiarity with ISO13485, 21 CFR Part 820, and other relevant regulatory frameworks.

Beckman Coulter Diagnostics, 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.

At Beckman Coulter Diagnostics 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 Beckman Coulter Diagnostics can provide.