QC Technician (m/f/d)

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 QC Technician is responsible for performing analysis on raw materials, semi-finished products or finished products as per established procedures and work instructions in compliance with good manufacturing/laboratory practices.

This position reports to the QC Lab Manager and is part of the Quality Control department located in Grens and will be an on-site role.

What you will do:

• Perform Quality Control inspection of components, semi-finished and finished products in compliance with good manufacturing/laboratory practices (GMP/GLP) . Interpret the results in comparison with established specification and edit quality control reports. In case of non-conformities, perform test result investigations for root cause and reports findings.

• These quality control consist on documentation, visual, dimensional and functional controls using 3D machines (Mitutoyo), Traction machine (Lloyd), caliper, ruler

• Perform several tasks in ISO7 environment (sampling, control)

• Manage non-conformity or change control in the area of competence in a dedicated computerized system. Write / update the Procedures and Work Instructions according to the needs of the evolution of the laboratory.

Who you are:

• CFC with professional maturity or equivalent diploma (such as BTS, DUT) with at least 3 year of experience in laboratory in medical devices or GMP / quality control field.

• Able to understand component drawings to use them as guidelines for component inspections

• Ease of use Microsoft Office, especially Excel

• Rigorous, analytical spirit and team player

• Fluent in French, intermediate technical English

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

• Visual management, Lean management or Operational Excellence

• 3D machine or Loyd machine

• ERP systems such as Oracle

• Basic knowledge in microbiology (environmental monitoring, Bioburden, BET)

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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