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 Danahers 15+ operating companies, our work saves livesand were all united by a shared commitment to innovate for tangible impact.

Youll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danahers 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 laboratorys 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 makingwe 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 Reagent QC Supervisor is responsible for leading the Reagent QC team supporting reagent manufacturing operations. This role is accountable for the daytoday performance and quality execution of the assigned QC team, ensuring work is completed in accordance with established procedures and quality system requirements.

The QC supervisor provides direct supervision, coaching, and operational oversight, supports consistent process execution, and escalates issues as needed. The role contributes to operational efficiency, quality outcomes, and talent development through effective team management and continuous improvement within defined departmental guidance.

This position reports to the Director Quality Assurance and is part of the Quality Control team located in Chaska, MN and will be an on-site role.

In this role, you will have the opportunity to:

• Supervise daily team activities to ensure work is completed accurately, on time, and in accordance with procedures
• Set daily and shortterm priorities, coordinating tasks and resources with other supervisors as needed
• Execute established policies and procedures, escalating issues that fall outside defined guidance
• Provide direct oversight, coaching, and feedback to team members to support performance and development
• Troubleshoot and resolve routine operational or technical issues using standard processes and judgment
• Support operational efficiency by applying basic business understanding and improving daytoday workflows
• Communicate expectations and information clearly, including handling routine performance or sensitive discussions

The essential requirements of the job include

• Education: High school diploma with 8+ years of relevant experience, or Bachelors degree with 5+ years, or Masters degree with 3+ years
• 3+ years of people management experience, preferably in a regulated manufacturing environment
• Experience with continuous improvement concepts and initiatives to improve quality outcomes
• Experience collaborating with crossfunctional teams

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

• Direct experience supporting FDA, ISO 13485, or notified body inspections, including serving as a frontroom or backroom lead
• Demonstrated experience implementing or sustaining Daily Management (DM) systems, including metrics, tiered huddles, and escalation paths

The salary range for this role is $95-105K This is the range that we, in good faith, believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole discretion unless and until paid and may be modified at the Companys sole discretion, consistent with the law.

Join our winning team today. Together, well accelerate the real-life impact of tomorrows 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.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or applyassistance@danaher.com.