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Qc Microbiologist Technician (M/F/D)

Posted on Dec. 6, 2024

  • Grens, Switzerland
  • No Salary information.
  • Full Time

Qc Microbiologist 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 Microbiologist Technician is responsible for performing Microbiological analysis on raw materials, semi-finished products or finished products as per established procedures and work instructions in compliance with good manufacturing/laboratory practices in a BSL-2 environment.

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 Bioburden analysis, Bacterial Endotoxins Test and Environmental Monitoring of ISO7 / ISO8 cleanrooms. Interpret these 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.

  • 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.

  • Perform analytical method validation or equipment qualification by writing protocols / reports and performing the tests.

Who you are:

  • CFC with professional maturity or equivalent diploma (such as BTS, DUT) with strong experience or Master’s degree in microbiology.

  • Minimum of 5 years of experience in laboratory in medical devices or GMP / quality control field / microbiology, backed up with fluency in French language as well as proficiency in Microsoft Office (especially Excel).

  • Good experience in Microbiology process, methods (Understanding of norms: ISO11737, ISO14644, ANSIAAMI ST72, USP<61>, USP<85>, USP<161>, EP 2.6.12, EP 2.6.14).

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

  • Ease of use in English.

  • Experience working with ERP systems such as Oracle.

#Li-onsite

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.

At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.


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