QC Project Lead: Analytical Methods & GMP Excellence

Lonza; Lavamünd; Vor Ort; Vertraulich; Vollzeit

Zusammenfassung

Lonza seeks a Manufacturing Science and Technology Expert - Drug Product (m/f/d) at 80–100% based in Visp, Switzerland. You will drive analytical method development, validation and transfer, ensure GMP compliance, and lead cross-functional teams for successful technology transfers across QC and production settings.

The role emphasizes analytical rigor, project leadership, and collaboration with R&D, QA, and external partners to deliver compliant, high-quality drug products.

Qualifikationen

• PhD or Master’s with substantial industry experience in analytical chemistry.
• Hands-on with chromatographic techniques (HPLC, GC).
• Experience in method development, validation, and transfer.

Aufgaben

• Lead QC/analytical projects from initiation to completion, defining scope and timelines.
• Develop, validate, and transfer chromatographic methods per ICH and GMP standards.
• Troubleshoot analytical instrumentation and implement CAPA actions.
• Ensure GMP/cGMP compliance, regulatory expectations, and quality standards.
• Coordinate with R&D, Production, QA and external labs to ensure project success.

Kenntnisse

Analytical chemistry

Project management

Team leadership

Ausbildung

PhD in Chemistry

MS/BSc with relevant experience

Tools

HPLC

GC

UV/Vis

KF

FTIR

Jobbeschreibung

Lonza seeks a Manufacturing Science and Technology Expert - Drug Product (m/f/d) at 80–100% based in Visp, Switzerland. You will drive analytical method development, validation and transfer, ensure GMP compliance, and lead cross-functional teams for successful technology transfers across QC and production settings.

The role emphasizes analytical rigor, project leadership, and collaboration with R&D, QA, and external partners to deliver compliant, high-quality drug products.