Verification Engineer

Danaher Corporation•Chaska, MN

1d•Onsite

About The Position

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. The Verification Engineer is responsible for all verification and validation activities for the Immunoassay product line. This includes instrument maintenance, drafting and execution of verification and validation test protocols, and working with the broader R&D team to support verification and validation activities. This position will be an on-site role in Chaska, Minnesota and reports to the Verification and Validation Manager as part of the Global Systems V&V Organization.

Requirements

Bachelor’s degree and 0-2 years experience in Science, Engineering or related field
Ability to execute test protocols in a laboratory setting
Strong attention to detail and understanding of regulated documentation practices

Nice To Haves

Previous experience in Medical device, biotech, or FDA regulated environments

Responsibilities

Create verification and validation test plans in support of new product development and continuous delivery of hardware and software design
Write and Execute verification and validation test protocols following approved procedures and documentation standards.
Work with the broader R&D team to support verification and validation activities