On-Site GMP QC Specialist (7-Month)

Lonza Group AG; Eyholz; Vor Ort; CHF 80.000 - 100.000; Vollzeit

Zusammenfassung

Lonza Group AG in Eyholz (VS) is seeking a Quality Control Specialist for a 7-month assignment (41 hours/week). You will act as the operational backbone for client campaigns, manage compliance workflows, and track projects to deliver high-quality biopharmaceuticals.

The role is site-based with limited flexibility to work on site. Ideal candidates hold a Master’s or PhD in Life Sciences, have GMP QC experience, and are fluent in English; German is a strong asset.

Qualifikationen

• Master's or PhD in Biology, Biochemistry, Pharmacy, or related Life Sciences.
• Familiar with GMP-regulated QC processes.
• Experience with laboratory software systems (LIMS, TrackWise, Documentum).

Aufgaben

• Drive operational excellence by maintaining clear customer communication and supporting the preparation and oversight of manufacturing campaigns.
• Ensure strict GMP compliance through active management of change requests and deviation investigations.
• Support key quality milestones by assisting during customer audits and regulatory inspections.
• Coordinate daily QC activities, prioritizing tasks to keep project timelines on track.
• Collaborate with production, quality assurance, and laboratory teams to ensure seamless campaign execution.
• Contribute to continuous improvement initiatives within the local QC unit.

Kenntnisse

English proficiency

German language skills

Organizational skills

Team collaboration

Ausbildung

Master's or PhD in Biology/Biochemistry/Pharmacy

Tools

LIMS

TrackWise

Documentum

Jobbeschreibung

Lonza Group AG in Eyholz (VS) is seeking a Quality Control Specialist for a 7-month assignment (41 hours/week). You will act as the operational backbone for client campaigns, manage compliance workflows, and track projects to deliver high-quality biopharmaceuticals.

The role is site-based with limited flexibility to work on site. Ideal candidates hold a Master’s or PhD in Life Sciences, have GMP QC experience, and are fluent in English; German is a strong asset.