Biotechnologist Operator - 2-Shift Manufacturing cGMP

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile culture

Inclusive workplace

Competitive pay

Location benefits

Zusammenfassung

Lonza in Visp, Switzerland, is seeking Operators Biotechnologists with a Life Sciences background to support multiple business units in a GMP-regulated environment.

You will execute manufacturing activities in the Drug Product area, perform manual visual inspection of vials, provide frontline technical support, ensure batches comply with instructions and quality requirements, and prepare production documentation. Shift work is required.

Qualifikationen

• Experience in a GMP-regulated environment is required.
• Strong teamwork and collaboration across functions are essential.
• Excellent communication skills across multiple levels within the organization.

Aufgaben

• Execute manufacturing activities in the Drug Product area in accordance with cGMP guidelines, ensuring proper batch execution, troubleshooting issues, and providing recommendations for resolution.
• Perform manual visual inspection of liquid and lyophilized vials to identify and remove all defective units.
• Provide frontline technical and procedural support in collaboration with the manufacturing team.
• Ensure each batch is manufactured safely, on schedule, and in full compliance with batch instructions and quality requirements.
• Be responsible for the timely and high-quality preparation of required production documentation (e.g., MBRs, forms).
• Operate, set up, and clean production equipment and premises as required.

Kenntnisse

GMP experience

Team orientation

Communication skills

Flexibility

Jobbeschreibung

Lonza in Visp, Switzerland, is seeking Operators Biotechnologists with a Life Sciences background to support multiple business units in a GMP-regulated environment.

You will execute manufacturing activities in the Drug Product area, perform manual visual inspection of vials, provide frontline technical support, ensure batches comply with instructions and quality requirements, and prepare production documentation. Shift work is required.