T2 Production Operations
Beckman Coulter Diagnostics

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 T2 Production Operations for Beckman Coulter Diagnostics is responsible for following established operation procedures, maintaining appropriate training records for your role, sustaining a smooth flow of material, and the execution of work orders to on-time completion.

This position is part of the Upstream Value Stream located in Chaska, MN, and will be on-site. In Upstream Value Stream, our goal is on-time delivery of cell culture, purifications, and conjugations to support on-time delivery of immunoassays to patients.

You will be a part of the Upstream Value Stream focusing on Cell Culture, Purifications and/or Conjugations. If you thrive in a fast-paced dynamic role and want to work to build a world-class manufacturing organization-read on.

In this role, you will have the opportunity to:

• Execute the daily production plan to due date conformance and quality standards according to Standard Operating Procedures (SOPs)
• Independently execute work regarding protein purifications and/or conjugations using good laboratory practices; assistance in other areas as needed
• Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP), and ISO regulatory requirements
• Apply basic analytical skills or scientific methods to perform daily tasks
• Work directly and cooperatively with cross-functional team members to troubleshoot issues and ensure emphasis on quality

The essential requirements of the job include:

• Must have the minimum requirement of an AA degree with 1+ year of related experience.
• Demonstrating good laboratory practices

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

• A regulated industry preferred (e.g. FDA, ISO)

Join our winning team today. Together, we'll 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.

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. 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.

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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 applyassistance@danaher.com to request accommodation.