Supervisor Quality Control

Danaher•Chaska, MN

17h•Onsite

About The Position

At Beckman Coulter Diagnostics, one of Danaher’s 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 Reagent QC Supervisor is responsible for leading the Reagent QC team supporting reagent manufacturing operations. This role is accountable for the day‑to‑day 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.

Requirements

High school diploma with 8+ years of relevant experience, or Bachelor’s degree with 5+ years, or Master’s 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 cross‑functional teams

Nice To Haves

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

Responsibilities

Supervise daily team activities to ensure work is completed accurately, on time, and in accordance with procedures
Set daily and short‑term 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 day‑to‑day workflows
Communicate expectations and information clearly, including handling routine performance or sensitive discussions