Lead QC Microbiology Scientist - GMP Method Validation

Seeds Renewables; Schweiz; Vor Ort; EUR 118.241 - 161.238; Vollzeit

Zusammenfassung

Eurofins Schweiz is seeking a QC Microbiology Scientist for driving projects that introduce and validate microbiological analytical methods within our GMP-regulated QC laboratory in Switzerland. You will lead method development, coordinate with QA and external suppliers, and ensure GMP compliance across timelines and deliverables.

The role requires technical expertise in analytical methods, QA collaboration, device qualification documentation, and staff training to support site expansion and

Aufgaben

• Lead projects implementing new analytical methods and equipment in the microbiological lab (e.g. identification methods, utility testing).
• Plan and coordinate with internal and external stakeholders (QA, customer service, 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 for equipment qualification (URS, QP, DQ, IOQ) and method validation/transfer (protocol, reports).
• Train and mentor laboratory staff.
• Supervise customer projects focusing on utility qualification testing and related subcontracted services.
• Plan and organize customer projects and deliverables (review of documents, plans, validation reports).
• Map and configure projects in the LIMS system.
• Ensure work is carried out properly/on time with GMP-compliant execution.
• Approve analyses results and reports.
• Provide supervision and scientific support for ongoing projects and help acquire new ones.
• Handle laboratory deviations and root cause analyses (OOS).
• Contribute to general process optimization and site development.

Jobbeschreibung

Eurofins Schweiz is seeking a QC Microbiology Scientist for driving projects that introduce and validate microbiological analytical methods within our GMP-regulated QC laboratory in Switzerland. You will lead method development, coordinate with QA and external suppliers, and ensure GMP compliance across timelines and deliverables.

The role requires technical expertise in analytical methods, QA collaboration, device qualification documentation, and staff training to support site expansion and