QC Microbiology Technician — GMP Sterility & Bioburden

Incyte Corporation

Lavamünd

Hybrid

EUR 45.000 - 60.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
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Zusammenfassung

Incyte Corporation in Austria’s Kärnten region seeks a QC Microbiology Technician to support production release through microbiology testing, sterility testing with an isolator, and environmental monitoring in a GMP setting.

The role includes data review, method verifications/validations, CAPA support, and collaboration with QA, Engineering, and Validation. French and English language skills are required.

We value autonomy, analytical mindset, and participation in digitalization initiatives.

Qualifikationen

  • Degree in Microbiology (CFC or higher) with at least 5 years in biotech/pharma.
  • Hands-on Bioburden and LAL testing experience.
  • Sterility testing of aseptically filled drug product (DP) using an isolator.
  • Strong knowledge of GMP, data integrity and documentation.
  • Experience with deviations, root cause analysis and CAPA implementation.

Aufgaben

  • Perform QC analysis to support production release of drug substance (Bioburden, LAL).
  • Perform sterility testing of aseptically filled drug product (DP) using an isolator.
  • Sampling and testing for environmental monitoring and utilities control.
  • Review analytical data, calculations and reports with traceability and integrity.
  • Collaborate cross-functionally to support investigations and CAPAs.
  • Participate in improvement projects to increase lab efficiency and compliance.

Kenntnisse

Bioburden testing
LAL testing
Sterility testing
Environmental monitoring
Data review
CAPA implementation
Cross-functional collaboration
Autonomy
French (fluent)
English knowledge

Ausbildung

Degree in Microbiology (CFC or higher)

Tools

Microsoft Office

Jobbeschreibung

Incyte Corporation in Austria’s Kärnten region seeks a QC Microbiology Technician to support production release through microbiology testing, sterility testing with an isolator, and environmental monitoring in a GMP setting.

The role includes data review, method verifications/validations, CAPA support, and collaboration with QA, Engineering, and Validation. French and English language skills are required.

We value autonomy, analytical mindset, and participation in digitalization initiatives.

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