Associate Scientist QC

Are you ready to play a key role in maintaining the highest quality standards in pharmaceutical manufacturing? We are looking for a Temporary Associate Scientist - QC to lead lab investigations and manage minor deviation reports at our Visp site.

This is a fully site‑based role. 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:

• Contribute directly to patient safety and product quality by ensuring robust resolution of laboratory events and investigations.

• Collaborate closely with laboratory analysts, supervisors, and Quality Assurance (QA) stakeholders across the Visp site.

• Perform root cause analysis and author minor deviation reports, Out of Specification (OOS), and System Suitability Test (SST) failure investigations.

• Retrieve, organize, and review analytical raw data from electronic systems such as LIMS and Chromatographic Data Systems (CDS).

• Ensure analytical raw data corrections strictly follow GMP and data integrity requirements.

• Maintain comprehensive, compliant, and inspection-ready laboratory documentation.

• Drive continuous improvement initiatives related to lab documentation practices and investigation workflows.

What we are looking for:

• Educational background in Chemistry, Biochemistry, Life Sciences, Pharmaceutical Sciences, or equivalent relevant laboratory experience.

• Hands-on experience in a GMP-regulated pharmaceutical, biotechnology, or chemical manufacturing laboratory environment.

• Strong knowledge of GMP principles, data integrity standards, and root cause analysis methodologies.

• Proficiency with electronic laboratory systems, particularly LIMS and Chromatographic Data Systems (CDS).

• Fluency in English (written and spoken) is required; conversational German skills are highly preferred.

• Outstanding technical writing ability, analytical problem-solving capabilities, and sharp attention to detail.

• Ability to work independently on tight deadlines while maintaining excellent team communication.

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.

As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role.

Ready to play your part in shaping the future of life sciences? Apply now.