Senior Reagent Technician: M-F 2pm-10:30pm - Military Veterans

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 Production Technician 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 Reagent Manufacturing team 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 Reagent Pack Stream Team and report to the Supervisor Production Operations responsible for operating using Daily Management principles, providing immediate guidance and feedback to our associates, and focusing on daily, monthly, and quarterly objectives.  If you thrive in a team oriented, goal focused environment 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. 

• Train to Standard Operating Procedures (SOPs).  Follow engineering drawings, work order information, SOPs, and other written and verbal specifications in the manufacturing process while maintaining FDA requirements. 

• Perform the set-up, testing and troubleshooting of filling systems. 

• Assure compliance with FDA Quality System Regulations (QSR), Good Manufacturing Practices (GMP) and ISO regulatory requirements.

• Train new team members on equipment operations and work procedures as needed and provide procedural coaching, as needed.

• Identify, recommend, and implement quality improvements including but not limited to production methods, equipment performance, product quality and efficiencies.

The essential requirements of the job include:

• Must have a high school degree (or equivalent degree)

• Must have at least 5+ years relevant experience.

• Proficiency with Microsoft applications, including Word, PowerPoint, and Excel and the basic Windows operating system. 

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

• Experience in a regulated industry (e.g., FDA, ISO).