Process Validation Specialist — GMP & CPV Expert

Lonza; Oberwallis; Vor Ort; Vertraulich; Teilzeit

Zusammenfassung

Lonza in Visp is seeking a Process Validation Specialist to drive validation strategies for commercial manufacturing. You will prepare and execute validation protocols, document reports, and support CPV and PQR across the product lifecycle.

The role requires a PhD or Master’s in chemistry or chemical engineering, GMP experience, and strong analytical skills to manage multiple priorities in a fast-paced environment. English fluency is essential; German is a plus.

Qualifikationen

• PhD or Master's degree in chemistry, chemical engineering or related field.
• Experience in pharmaceutical or chemical manufacturing with GMP exposure.
• Strong analytical and problem-solving abilities; cross-functional collaboration.

Aufgaben

• Develop process validation strategies for commercial manufacturing processes.
• Prepare, execute, and document validation protocols and reports.
• Support CPV and PQR throughout the product lifecycle.
• Assess validation impact of deviations, investigations and change requests.
• Represent Process Validation in customer meetings and cross-functional projects.
• Act as SME during customer audits and regulatory inspections.
• Ensure compliance with cGMP and regulatory guidelines (ICH, FDA, EMA, PIC/S).

Kenntnisse

GMP experience

Analytical skills

Problem solving

Stakeholder management

Ausbildung

PhD or Master's in Chemistry or Chemical Engineering

Jobbeschreibung

Lonza in Visp is seeking a Process Validation Specialist to drive validation strategies for commercial manufacturing. You will prepare and execute validation protocols, document reports, and support CPV and PQR across the product lifecycle.

The role requires a PhD or Master’s in chemistry or chemical engineering, GMP experience, and strong analytical skills to manage multiple priorities in a fast-paced environment. English fluency is essential; German is a plus.