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Proclinical Logo Proclinical · Quality Control

QC Associate

Switzerland, Visp · Job Posted March 19, 2026
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Job Description

Join a leading Swiss team as a QC Associate driving excellence in biopharmaceutical quality control. Proclinical is seeking a QC Associate to join a dynamic team in Switzerland. In this role, you will focus on quality control activities related to biopharmaceutical products intended for clinical and commercial use. This position requires adherence to GMP and safety guidelines, with an emphasis on biochemical analytics.

Job Responsibility

  • Plan and contribute to the execution of release analytics for biopharmaceutical products
  • Implement, optimize, transfer, and validate analytical methods, particularly in biochemical analysis
  • Provide technical expertise for analytical and technical inquiries
  • Extract, analyze, and interpret analytical data, as well as prepare reports and presentations
  • Manage change requests and deviations in compliance with GMP standards
  • Create, review, and approve documentation to ensure regulatory compliance
  • Ensure quality, timeliness, and cost-effectiveness in assigned tasks while maintaining close collaboration with other QC groups, research, production, and quality assurance teams

Requirements

  • Strong knowledge of GMP guidelines and quality control processes
  • Expertise in biochemical analytics and analytical method validation
  • Ability to manage and interpret complex analytical data
  • Proficiency in creating and reviewing technical documentation
  • Effective communication and collaboration skills across teams
  • Self-motivated with the ability to work independently within project frameworks
  • Must have the right to work in this location or hold an EU passport
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