Drug Product Process Expert – Relocation Supported

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Motivated and inclusive team

Up-to-date production line progress

Agile career and dynamic working style

Ethical workplace

Compensation programs recognizing high

Variety of role-dependent benefits

Zusammenfassung

Lonza in Visp, Switzerland, is seeking a Manufacturing Process Expert – Drug Product 80-100% (f/m/d). You will provide frontline technical support on drug product manufacturing, ensuring cGMP compliance and high-quality batch execution across the shopfloor.

You will lead process improvement projects, own investigations and CAPAs, and collaborate with manufacturing, engineering and QA to drive safe, timely production and accurate electronic batch records.

Qualifikationen

• 3-5 years of experience in sterile manufacturing operations.
• Familiar with GMP, SOPs, deviations management.
• Fluent in English; German is an advantage.
• Good communication across interfaces and teams.
• Structured, proactive and organized work approach.

Aufgaben

• Provide frontline technical and procedural support to shopfloor in Drug Product per cGMP.
• Drive process improvement projects in manufacturing.
• Establish timely and high-quality production documentation (eBDRs, GMP docs).
• Own process-related investigations and CAPAs with timely resolution.
• Train and serve as SME to other departments.

Kenntnisse

Effective communication

Cross-functional collaboration

Structured problem solving

Proactive / solution-oriented

Fluent in English

Ausbildung

Bachelor/Master in Pharmaceutical Technology, Chemistry, Pharmacy

Tools

Trackwise

SAP

MES

Jobbeschreibung

Lonza in Visp, Switzerland, is seeking a Manufacturing Process Expert – Drug Product 80-100% (f/m/d). You will provide frontline technical support on drug product manufacturing, ensuring cGMP compliance and high-quality batch execution across the shopfloor.

You will lead process improvement projects, own investigations and CAPAs, and collaborate with manufacturing, engineering and QA to drive safe, timely production and accurate electronic batch records.