Senior Technician Quality Control - 2nd Shift

    • Danaher Corporation
  • Chaska, MN
  • Posted 22 days ago | Updated moments ago

Overview

On Site
Full Time

Skills

Quality control
Medical devices
Life sciences
Value engineering
Science
Health care
Creativity
Reporting
Manufacturing
Computer hardware
INSPECT
Specification
Documentation
Design
Inspection
FDA
ISO 9000
IMPACT
Biotechnology
Law

Job Details

Wondering what's within Beckman Coulter Diagnostics? Take a closer look.

At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful.

Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at Danaher. Together, we're working at the pace of change to improve patient lives with diagnostic tools that address the world's biggest health challenges.

The Senior Technician Quality Control for Beckman Coulter Diagnostics is responsible for inspections on kits, in-process equipment, and/or finished products.

This position is part of the Quality Control Department located in Chaska, MN and will be onsite. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Quality Control Team and report to the Quality Control Supervisor of -Manufacturing-Hardware responsible for investigating and troubleshooting functionality and performance problems. If you thrive in a multifunctional, fast paced role and want to work to build a world-class Quality Control organization-read on.

In this role, you will have the opportunity to:
  • Inspect instruments during the build process to ensure components are within specification.
  • Inspect the final instrument.
  • Review and ensure all supporting documentation are within the Design History File.
  • Detailed record keeping of inspection documentation.
  • Work with a dedicated team of professionals.


The essential requirements of the job include:
  • High school degree (or equivalent degree) required.
  • 5+ years' experience in a related field


It would be a plus if you also possess previous experience in:
  • Providing informal guidance and support to more junior team members
  • Experience in a Medical Device, FDA, ISO regulated environment.


At Danaher we bring together science, technology and operational capabilities to 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. Our global teams are pioneering what's next across Life Sciences, Diagnostics, Biotechnology and beyond. For more information, visit .

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. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

The EEO posters are available here .

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.