Advanced Technician Production Operations
Description
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 Advanced Technician Production Operations for Beckman Coulter Diagnostics Co. Clare is responsible for the safe and efficient manufacture of immunoassay reagents for the IA immunoassay reagent kits.
This position is part of the Operations functions with Beckman Coulters and is located just outside Tulla in Lismeehan, O'Callaghan's Mills, Co. Clare 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 Immunoassay team and report to the IA Supervisor, Production Operations. If you thrive in an inclusive, dynamic, and multifunctional role and are a self-starter but also works well within a team with strong and positive communicate skills who wants to work to build a world-class manufacturing organization—read on.
In this role, you will have the opportunity to:
Manufacture immunoassay reagents within the Formulation Department in line with approved procedures and schedules.
Perform cleaning of tanks and operate, maintain, and support CIP systems and autoclave equipment.
Operate and maintain basic laboratory and production equipment, including analytical balances, pH meters, pipettes, spectrophotometers, and fume hoods.
Calibrate and perform routine maintenance on production equipment in accordance with procedures.
Maintain neat, accurate, and compliant documentation in line with GMP and Formulation procedures.
Ensure compliance with housekeeping, safety, environmental, and quality standards at all times.
Support audit readiness activities within the department and participate in inspections as required.
The essential requirements of the job include:
Leaving Certificate or equivalent
Experience in a regulated manufacturing or laboratory environment (e.g. diagnostics, medical device, pharmaceutical, or biopharma).
Experience following GMP, SOPs, and controlled documentation requirements.
Hands‑on experience operating laboratory or production equipment.
Experience maintaining production or laboratory records in compliance with quality systems.
It would be a plus if you also possess previous experience in:
Immunoassay, reagent, or kit manufacturing environments.
Equipment calibration, CIP systems, or autoclave operation.
Supporting audits or working in an inspection‑ready manufacturing environment.
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.