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.