12 Month Contract - Switzerland 

As a Visual Inspection Operator, you will play a critical role in ensuring the quality and safety of sterile drug products. You will be responsible for performing manual visual inspections of liquid and lyophilized vials, supporting manufacturing operations, and ensuring compliance with cGMP standards. This position requires attention to detail, adherence to quality procedures, and a strong commitment to patient safety.

Key Responsibilities

• Execute manufacturing activities in the Drug Product area according to cGMP guidelines, ensuring timely and compliant batch execution.
• Perform manual visual inspection of liquid and lyophilized vials to detect particulate matter and cosmetic defects.
• Provide frontline technical and procedural support to the manufacturing team.
• Ensure each batch is manufactured safely, on time, and in compliance with batch instructions and quality requirements.
• Prepare and maintain accurate production documentation (e.g., MBRs, forms, logbooks) for the assigned production area.
• Support process-related investigations and assist in decision-making on production issues.
• Contribute to process changes and CAPAs within required timelines.
• Participate in training activities and support onboarding of new team members.
• Operate, set up, and clean production equipment and maintain a clean working environment.

Qualifications & Skills

• Previous experience in a GMP-regulated environment (preferably in sterile drug product manufacturing).
• Fluent in English 
• Familiarity with GMP requirements, quality procedures, and SOP execution.
• Strong team orientation and good communication skills.
• Structured, focused, and well-organized working style.
• High motivation and dynamic drive.
• Willingness to work flexible hours and shift patterns (including weekends if required).