Location

TN Switzerland · Canton of Lucerne, Switzerland

Client / Employer

Lonza

Posted

Key Responsibilities

• Assignment in various functions within the production facilities in compliance with safety regulations and cGMP quality requirements.
• Recognition, interpretation and elimination of deviations.
• Execution of production steps incl. recording and calculations.
• Support in training of new team members.

Key Requirements

• Completed chemical / biopharmaceutical education.
• Professional experience in pharmaceutical production as an operator/production technician etc.
• Safety‑conscious work.
• Knowledge of process engineering.
• Willingness to work in shifts (e.g., 4‑shift pattern) with flexible work scheduling.