GMP Quality Control Lead - Biopharma Campaigns

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career culture

Inclusive workplace

Zusammenfassung

Lonza in Visp is seeking a Quality Control Specialist for a 7-month on-site assignment (41 hours per week). You will act as the operational backbone for client campaigns, ensuring GMP compliance and overseeing manufacturing campaigns.

The role requires a Master’s or PhD in Life Sciences, experience with QC processes in GMP, and familiarity with LIMS, TrackWise or Documentum. English fluent; German a plus.

Qualifikationen

• Master’s or PhD in Biology, Biochemistry, Pharmacy, or related Life Sciences field.
• Background with Quality Control in GMP-regulated environment.
• Hands-on lab software knowledge: LIMS, TrackWise, Documentum.
• Fluent English; German language skills are a strong asset.
• Strong organization and ability to prioritize dynamic project demands.

Aufgaben

• Drive operational excellence by maintaining clear customer communication and supporting 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.
• Calculate, monitor, and report QC project costs to maintain financial alignment.
• Collaborate with production, QA, and laboratory teams to ensure seamless campaign execution.
• Contribute to continuous improvement initiatives within the local QC unit.

Kenntnisse

GMP compliance

QC processes

LIMS

TrackWise

Documentum

English fluency

German language

Ausbildung

Master's in Life Sciences

PhD in Life Sciences

Tools

LIMS

TrackWise

Documentum

Jobbeschreibung

Lonza in Visp is seeking a Quality Control Specialist for a 7-month on-site assignment (41 hours per week). You will act as the operational backbone for client campaigns, ensuring GMP compliance and overseeing manufacturing campaigns.

The role requires a Master’s or PhD in Life Sciences, experience with QC processes in GMP, and familiarity with LIMS, TrackWise or Documentum. English fluent; German a plus.