GMP – Laboratory Technician Switzerland

Resourcing Life Science; Indiana (PA); On-site; USD 45,000 - 65,000; Full time

Job summary

Resourcing Life Science is seeking a Laboratory Technician in Indiana, Pennsylvania. The role involves executing laboratory tests, method development, and maintaining documentation.

The ideal candidate has at least 2 years of experience in the pharmaceutical or biotech industry, GMP experience, and knowledge of data integrity protocols. Proficiency in chromatography software like OpenLab EZ Chrome or Chromeleon is a plus, with fluency in German and good English skills also required.

Qualifications

• Minimum 2 years as a Laboratory Technician in the pharmaceutical or biotech industry.
• Experience in GMP compliance.
• Knowledge of data integrity protocols.

Responsibilities

• Executing laboratory tests for method development and documentation.
• Performing method verifications for raw materials and finished products.
• Coordinating analytical testing for investigations and troubleshooting.

Skills

Laboratory Technician experience

GMP experience

Data integrity knowledge

Chromatography software proficiency

Fluent in German

Good knowledge of English

Tools

OpenLab EZ Chrome

Chromeleon

Job description

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