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Main tasks

Tasks and responsibilities

  • Executing laboratory tests for method development, optimization, validation, and transfer while maintaining accurate and timely documentation.
  • Performing method verifications for raw materials and finished products according to pharmacopoeial standards.
  • Coordinating analytical testing to support deviation investigations, troubleshooting, and change management.
  • Managing the documentation and processing of laboratory deviations, OOX results, and CAPA measures.
  • Maintaining primary responsibility for the operation and upkeep of assigned laboratory equipment.
  • Ensuring all work processes consistently meet established data integrity requirements.

Qualifications

  • Min 2 years as Laboratory Technician in the pharmaceutical / chemical or biotech industry or other comparable experience in the industrial or pharmaceutical sector
  • Min 2 years in GMP experience
  • Fundamental knowledge of data integrity protocols and conducting audit trail reviews.
  • Experience in laboratory equipment qualification and method validation is highly desirable.
  • Proficiency in OpenLab EZ Chrome or Chromeleon chromatography software is an advantage.
  • Fluent in German and good knowledge of English

Tagged as: qa jobs

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