Quality Control Technician

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

Bring more to life. Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cytiva, 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.
Working at Cytiva means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. Take your next step to an altogether life-changing career.
Learn about the Danaher Business System which makes everything possible.
The Quality Control Technician is responsible for performing in-process testing and inspections of medical devices to ensure compliance with quality standards and specifications in a fast-paced manufacturing environment. We are seeking a detail-oriented and proactive technician who can effectively manage multiple tasks and work efficiently under pressure.
This position reports to the Quality Control Manager and is part of the Quality Control department located in Cardiff and will be an on-site role working on a shift pattern. The shift pattern is 6am - 2pm and 2pm - 10pm on a weekly rotation.

• Operate testing equipment effectively according to the Work Instructions, hourly targets and safety requirements
• Document and report test results, ensuring that non-conformances are reported accurately and promptly when they occur.
• Collaborate with production and engineering teams to identify and resolve quality issues
• Maintain a clean and organised work area to ensure a safe and efficient working environment

• Minimum of 1 years’ experience working in a manufacturing facility or similar
• Ability to work well under pressure with minimal supervision, using own initiative.
• Excellent attention to detail and highly motivated, with a strong focus on safety, quality and delivery.

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

• Proficient in using measurement tools and inspection equipment
• Previous experience within a quality control environment/ ISO 9001/ ISO
  13485/ Pharma regulated manufacturing environment is an advantage.
• Able to make reasoned and objective decisions where necessary

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.

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