Sterile Drug Product Technician — 3 Shifts

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Zusammenfassung

Lonza in Visp, Switzerland, seeks personnel for drug product manufacturing. You will execute GMP batch production, support investigations, maintain batch records, and participate in training.

The role requires flexibility for 3 shifts, including nights and Saturdays, with a focus on quality and safety. Fluent English is essential (German a plus); experience in GMP environments and SAP/MES familiarity is beneficial.

Qualifikationen

• Several years of GMP shopfloor experience, preferably sterile Drug Product manufacturing.
• Fluent in English; German is a plus.
• Familiarity with GMP requirements, quality procedures and SOP execution.
• Strong team orientation and effective communication across interfaces.
• Structured, focused and well organized working attitude.
• High motivation and dynamic drive.
• IT knowledge including SAP and MES is beneficial.
• Willingness to work in a 3-shift pattern including nights and Saturdays.

Aufgaben

• Executes manufacturing activities in the Drug Product area.
• Ensure batch execution per cGMP, evaluate test results, troubleshoot equipment.
• Provide frontline technical and procedural support to the manufacturing team.
• Secure safe, on-time production in compliance with batch instructions and quality.
• Prepare, execute and review batch records and GMP documents for the area.
• Support process investigations and decisions on production issues.
• Assist CAPAs and process changes with required timelines.
• Perform training of operators and onboard new joiners.
• Operate, set up and clean production equipment and premises for liquid and freeze-dried drug forms.

Kenntnisse

GMP experience

Team orientation

Effective communication

Structured approach

Motivation & drive

SAP knowledge

MES knowledge

Shift work readiness

English proficiency

Tools

SAP

MES

Jobbeschreibung

Lonza in Visp, Switzerland, seeks personnel for drug product manufacturing. You will execute GMP batch production, support investigations, maintain batch records, and participate in training.

The role requires flexibility for 3 shifts, including nights and Saturdays, with a focus on quality and safety. Fluent English is essential (German a plus); experience in GMP environments and SAP/MES familiarity is beneficial.