Quality Analyst (m/w/d)

Tasks :

• Carry out biochemical analysis and supervision activities according to current laboratory procedures, in compliance with GMP/GDP rules and/or projects related to the Quality Control department’s activities.

• Comply with all current procedures.

• Comply with and apply EHS rules.

• Complete various forms, logbooks, and documents in compliance with Good Manufacturing and Documentation Practices, as well as ALCOA+ principles.

• Inform the Supervisor immediately (the same day, verbally and/or in writing) in the event of non-compliant and/or invalid results, and initiate the event in the quality system within the required timeframes.

• Handle laboratory investigations.

• Follow planning requirements and proactively report any issues.

• Execute qualification protocols for reagents/consumables and validation (methods, systems, equipment).

• Ensure that equipment calibration and maintenance are up to date before analysis.

• Follow Kanban management in real time.

• Report deviations from procedures to the method/equipment manager and the Supervisor/delegate/Expert.

• Be able to identify and resolve some less complex problems related to your area of expertise (troubleshooting).

• Prepare solutions or approve solutions in the laboratory.

• Organize and maintain the laboratory in general, following 5S standardization norms.

• Support continuous improvement initiatives.

Qualification:

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

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

• Experience in electrophoresis, HPLC, ELISA, or enzyme activity determination is desired.

• Fluent French and technical English.

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

Requirements: