Quality Control Specialist

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

Quality Control Specialist

Lonza Group AG
Vacant since : 10.09.2026
3930 Eyholz (VS)
80% - 100%
By agreement
Temporary

Quality Control Specialist
Quality Control Specialist
Join our team in Visp as a Quality Control Specialist for a 7-month assignment (41 hours/week), where you will serve as the operational backbone for critical client campaigns, handling compliance workflows and project tracking to help deliver life-changing biopharmaceuticals.
Site-based with limited flexibility
This role is primarily based on site. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.
What you will get:
An agile career and dynamic working culture.
An inclusive and ethical workplace.
What you will do:
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, independently prioritizing tasks to keep project timelines on track.
Calculate, monitor, and report on QC project costs to maintain financial alignment.
Collaborate cross-functionally with production, quality assurance, and laboratory teams to ensure seamless campaign execution.
Contribute to continuous improvement initiatives within the local QC unit.
What we are looking for:
Master's or PhD in Biology, Biochemistry, Pharmacy, or a related Life Sciences field.
Background or familiarity with Quality Control processes in a GMP-regulated environment.
Hands-on experience or working knowledge of laboratory software and systems such as LIMS, TrackWise, or Documentum.
Professional fluency in English (written and spoken) is required; German language skills are a strong asset.
Strong organizational and time-management skills with the ability to prioritize dynamic project demands.
A reliable, team-oriented mindset with excellent communication skills for stakeholder and customer interactions.
Ability to step in quickly and thrive in a fast-paced CDMO environment under tight deadlines.
About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment.

• Work location 3930 Eyholz (VS)
• Workload 80% - 100%
• Employment start By agreement
• Employment duration Temporary