QC Microbiology Technician – GMP & Automation

Incyte

Yverdon-les-Bains

Vor Ort

CHF 90.000 - 120.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine zielgenaue Bewerbung für diese Stelle — ein maßgeschneiderter Lebenslauf und ein Anschreiben, die genau zur Stellenanzeige passen.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

Incyte in Yverdon-les-Bains, Switzerland, seeks a QC Microbiology Technician to support production release and sterility testing using an isolator. You will perform Bioburden, LAL testing, environmental monitoring, and contribute to method verification/validation within a GMP environment.

You will review data, maintain SOPs, drive continuous improvement, and collaborate with QA, Engineering and Validation. French fluent and English good, 5+ years in biotech QC preferred.

Qualifikationen

  • 5+ years in biotech/pharmaceutical QC microbiology in GMP setting.
  • Hands-on Bioburden and LAL testing experience.
  • Experience with sterility testing using an isolator.
  • Knowledge of GMP data integrity principles.
  • Strong cross-functional collaboration and communication.

Aufgaben

  • Performs QC analysis to support production release of drug substance (Bioburden, LAL).
  • Performs sterility testing of aseptically filled drug product using an isolator for DP batch release.
  • Performs sampling and testing for environmental monitoring and utilities control.
  • Ensures adherence to GMP, data integrity, safety, and internal quality standards.
  • Executes microbiology method verification/validation activities.

Kenntnisse

Bioburden
LAL
Sterility testing
Environmental monitoring
Data integrity
CAPA
GMP documentation
Cross-functional collaboration
Process optimization
Digitalization

Ausbildung

Microbiology degree (CFC or higher)

Tools

Isolator
LIMS

Jobbeschreibung

Incyte in Yverdon-les-Bains, Switzerland, seeks a QC Microbiology Technician to support production release and sterility testing using an isolator. You will perform Bioburden, LAL testing, environmental monitoring, and contribute to method verification/validation within a GMP environment.

You will review data, maintain SOPs, drive continuous improvement, and collaborate with QA, Engineering and Validation. French fluent and English good, 5+ years in biotech QC preferred.

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