Technician 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 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 Technician Production-Operations for Beckman Coulter Diagnostics is responsible manufacturing control and calibration products in a Food and Drug Administration (FDA)-regulated environment. In this role, you will perform In-Process testing and calculations of our products to determine acceptance ranges for Beckman Coulter Inc. (BCI) Flow Cytometers (instruments such as FC-500, AQUIOS and NAVIOS).

This position is part of the Reagents Manufacturing Department located in Hialeah, FL and will be on-site. At Beckman Coulter, our vision is to relentlessly reimagine healthcare, one diagnosis at a time.

You will be a part of the Reagents Manufacturing team and report to the Reagents Manufacturing Supervisor. If you thrive in a fast-paced, multifunctional role and want to work to build a world-class Supply Chain a fast-paced, multifunctional role and want to work to build a world-class Supply Chain organization-read on.

In this role, you will have the opportunity to:

• Compile and analyze test information to determine whether the process or equipment is operating efficiently and to diagnose malfunctions.

• Use relevant information and Critical Thinking skills to determine product and process compliance with the Quality System Regulations.

• Drives Continuous Process Improvement and contributes technical expertise and direction for root-cause analysis of product issues as well as implementation and sustainment for product issue remediation.

The essential requirements of the job include:

• High School Degree (or equivalent degree) and 2+ years experience working in an FDA-regulated environment/laboratory.

• Prior experience in manufacturing or assembly line work/machinery, and ability to read and interpret technical documents.

• Ability to lift 50 pounds with or without assistance and stand 6 to 7 hours a day.

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

• Basic troubleshooting skills to identify minor issues with machinery and ability to read and interpret technical documents.

• The position requires concentration for long periods and good hand-eye coordination when working in assembly line process.

• Ability to perform basic math for keeping accurate levels of inventory and for documenting defects or issues that occur in the operation.