Intern Quality Control Bioanalytics 80-100%

Lonza; Lavamünd; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career

Inclusive workplace

Compensation programs

Benefits by role/location

Zusammenfassung

Lonza Visp invites you to join the QC Bioanalytics internship to gain hands-on experience in a GMP-regulated laboratory. You will support routine analyses with ELISA and qPCR, and help document results and write work instructions.

This fully site-based role offers close collaboration with a dynamic team, exposure to quality control operations, and a practical introduction to pharmaceutical manufacturing, with a focus on accuracy, safety, and compliance.

Qualifikationen

• GMP-regulated environment experience is an asset.
• Completed vocational training in biology or related field.
• Experience with ELISA or qPCR is advantageous.
• Independent, responsible, and precise with good teamwork.

Aufgaben

• Carrying out routine analysis with a focus on ELISA and qPCR, in compliance with GMP and safety guidelines
• Method implementation, validation and method transfer
• Administrative activities, such as documenting the results and creating work instructions
• Support laboratory maintenance (responsibility for equipment) and ensure that the laboratory is clean and tidy

Kenntnisse

Teamwork

Independent work

Communication

Ausbildung

Biology Laboratory Technician vocational training

Bachelor's degree in Biology

Tools

ELISA

qPCR

Jobbeschreibung

The actual location of this job is in Visp, Switzerland.

We are looking for an Intern (m/f/d) in QC Bioanalytics. The QC Bioanalytics department at Lonza Visp is responsible for a broad range of biochemical analyses. To support our growing team, we are seeking a motivated intern (m/f/d) who is eager to gain hands‑on experience in a GMP‑regulated laboratory environment and contribute to our quality control operations.

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.
• Compensation programs that recognize high performance.
• A variety of benefits dependent on role and location.

What you’ll do:

• Carrying out routine analysis with a focus on ELISA and qPCR, in compliance with GMP and safety guidelines
• Method implementation, validation and method transfer
• Administrative activities, such as documenting the results and creating work instructions
• Support laboratory maintenance (responsibility for equipment) and ensure that the laboratory is clean and tidy

What we are looking for:

• Completed vocational training as a Biology Laboratory Technician (m/f/d), a Bachelor's degree in Biology, or an equivalent qualification
• Experience working in a GMP-regulated environment is considered an asset
• First experience with ELISA and qPCR is advantageous
• Experience working in a GMP-regulated environment is considered an asset
• You are independent, responsible and have a very precise way of working. You have good communication and teamwork skills and enjoy interdisciplinary collaboration
• You enjoy being part of a young, dynamic team, are committed and have initiative
• Fluent in either German or English (language skills in the respective other language is a plus)

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 for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.