CIT Specialist Software

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Beckman Coulter Diagnostics, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact. You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

As a global leader in clinical diagnostics, Beckman Coulter Diagnostics has challenged convention to elevate the diagnostic laboratory’s role in improving patient health for more than 90 years. Our diagnostic solutions are used in routine and complex clinical testing, and are used in hospitals, reference and research laboratories, and physician offices around the world. Every hour around the world, more than one million tests are run on Beckman Coulter Diagnostics systems, impacting 1.2 billion patients and more than three million clinicians per year.

The Clinical IT Specialist is responsible for coordinating and executing all activities related to the implementation, configuration, validation, and support of Beckman Coulter’s Clinical IT solutions in customer laboratories.

Experience in In Vitro Diagnostics (IVD) environments is essential for success in this role. You will work directly within regulated laboratory settings, supporting diagnostic instruments, integration platforms and information systems. This requires an understanding of IVD workflows, quality systems, regulatory compliance, and the critical nature of diagnostic data in patient care.

You will be part of the Clinical IT Europe team, reporting to the Clinical IT Manager. This role partners closely with upstream teams (Product) and downstream functions (Sales, Marketing, Project Management), while playing a key role in post‑sales support across the Beckman Coulter Clinical IT portfolio.

In This Role, You Will:

• Deploy and configure Total Laboratory Automation solutions in accordance with approved designs, project timelines, and customer requirements
• Maintain rigorous control of projects, including documentation, reporting, and compliance with quality standards
• Proactively manage risks and issues during implementation, identifying corrective actions to meet project milestones
• Build and sustain strong customer relationships through continuous engagement and solution‑driven support
• Act as a trusted consultant for customers and internal stakeholders, including Pre‑Sales teams

The essential requirements of the job include:

• Degree or Higher Education Level in Biomedical engineering or equivalent with Hands‑on experience in In Vitro Diagnostics (IVD)
• Proven ability to self‑organize, manage competing priorities, and perform in a demanding environment
• Languages: Fluent English with one additional EMEA language an advantage

Travel & Physical Requirements:

• Flexibility to travel 50–70% within UK & Ireland, with additional travel across Europe as business needs require
• Must have a valid driver’s license with an acceptable driving record

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

• Experience with networking, virtual environments (Hyper‑V, VMware), and Windows Server (2025, 2022, 2019)
• Knowledge of laboratory analyzer connectivity and communication protocols (HL7, ASTM)
• Experience working within a European or international team

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