Eurofins Scientific is a leading international life sciences company providing a unique range of analytical testing services across multiple industries to make life and our environment safer, healthier, and more sustainable. From the food you eat to the water you drink and the medicines you rely on, Eurofins laboratories support many of the world’s largest companies in ensuring product safety, ingredient authenticity, and accurate labeling.
As part of its commitment to society and the planet, Eurofins delivers testing services that protect public health while upholding strong corporate responsibility standards. This includes a dedicated focus on environmental sustainability as well as fostering diversity, equity, and inclusion across its global network.
Eurofins Bio Pharma Product Testing offers complete CMC Testing Services for the Bio/Pharmaceutical industry, including all starting materials, process intermediates, drug substances, drug product, packaging, and manufacturing support through our broad technical expertise in Biochemistry, Molecular & Cell Biology, Virology, Chemistry and Microbiology.
Our local presence ensures personal service backed by a unique global breadth of harmonised capabilities that support all functional areas of bio/pharmaceutical drug development and manufacturing, including method development, microbiology, process validation and quality control.
Job Description
We are looking for a QC Microbiology Scientist for driving projects that introduce and validate innovative microbiological analytical methods within our GMP-regulated QC laboratory who will contribute to the significant growth of our business in Switzerland by:
Lead projects focused on the implementation of new analytical methods and new equipment into the microbiological laboratory (e.g. identification methods, utility testing).
Plan and coordinate with internal (e.g. QA, customer service) and external stakeholders (e.g. supplier).
Ensure compliance with GMP, regulatory guidelines, and internal quality standards.
Manage project timelines, resources, and deliverables.
Provide technical expertise on analytical methods.
Prepare and review documents related to equipment qualification (URS, QP, DQ, IOQ) and method validation and