Tasks :

• Perform biochemical analysis and supervision activities according to laboratory procedures, adhering to GMP/BPD regulations and/or projects related to the Quality Control department’s activities.

• Comply with all applicable procedures.

• Adhere to and apply EHS rules.

• Accurately complete various forms, logbooks, and documents in accordance with Good Manufacturing and Documentation Practices (GMP/GLP) and ALCOA+ principles.

• Immediately inform the Supervisor of non-conforming and/or invalid results verbally and/or in writing on the same day and initiate the event in the quality system within the specified timelines.

• Manage laboratory investigations.

• Follow planning requests and proactively report any issues.

• Execute reagent/consumable qualification and validation protocols (method, system, equipment).

• Ensure calibration and maintenance of equipment are up to date during analysis.

• Manage Kanban processes in real-time.

• Report procedural deviations to the Method/Equipment Manager and Supervisor/Delegate/Expert.

• Identify and resolve some less complex issues related to your area of expertise (troubleshooting).

• Prepare solutions or approve laboratory solutions.

• Maintain and organize the laboratory in general, adhering to 5S standardization norms.

• Support continuous improvement initiat ives.

Qualification:

• Minimum education level: CFC laboratory technician in biology or another relevant scientific field.

• At least 3 years of experience in a Quality Control laboratory in a cGMP environment.

• Experience in electrophoresis analysis, HPLC, ELISA, or enzymatic activity determination is preferred.

• Fluent French and technical English.

• Swiss or EU nationality, or a valid Swiss work permit.

Requirements:

Start : 01.01.2025