The Life Science Career Network

CTC are specialized industry experts who help companies source the best talent and provide reliable HR and consulting services. We support diverse candidates in finding promising career opportunities and offer the latest in skill development training programs.

About the Client

Our client is a specialist biotherapeutics manufacturer with over a century of experience treating various diseases worldwide. They are committed to patients with coagulation disorders, immunological diseases, enzyme deficiency diseases, and other rare diseases.

Position Overview

We are seeking a Quality Control Analyst for a 12-month contract position at our client's headquarters in Bern. The role involves managing small projects, developing and optimizing biochemical methods, executing experimental plans, conducting tests, authoring documentation, and participating in investigations and project meetings, all while adhering to cGMP and data integrity principles.


  • Manage and deliver small projects and project deliverables.
  • Develop, optimize, and/or validate methods specific to biochemistry.
  • Develop experimental plans, including estimating materials, resources, and time required.
  • Execute appropriate testing and experimental plans as required.
  • Author, review, and update protocols, reports, test procedures, and associated documentation.
  • Contribute subject matter expertise during the investigation of deviations, atypical results, and method performance issues.
  • Actively participate in project meetings and regulatory submissions as required.
  • Ensure timely communication and completion of deliverables while adhering to cGMP and data integrity principles.

Minimum Requirements:

  • Master’s degree in Biological Science or a related technical field (Doctoral degree preferred or equivalent industry experience of 3+ years).
  • At least 1 year of experience in method development/validation for the assessment of biological pharmaceutical products, or equivalent post-graduate experience.
  • Experience in cGMP Quality Control is a plus.
  • Strong experience in immunoassays, cell-based assays, and electrophoretic techniques.
  • Proven written and verbal communication skills.
  • Good problem-solving skills.
  • Excellent knowledge of English and German.
  • Ability to operate independently and as part of a team.
  • Flexibility to manage changing priorities.

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