15 English-speaking jobs in Visp

Senior Category Manager and Buyer - Automation Are you ready to shape the future of pharmaceutical manufacturing technology? Join our global procurement team to drive strategic automation sourcing that directly supports the production of life-saving medicines. Site‑based role This role is primarily based on site.

DeltaV Automation Engineer 80-100% (m/f/d) Relocation assistance is available for eligible candidates and their families, ensuring a smooth transition to our welcoming community in Visp. Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it.

Production Engineer Production Engineer - Small Devices Ensure the operational readiness and reliability of small manufacturing equipment at our BioAtrium facility in Visp, directly supporting the delivery of life-changing biopharmaceuticals. This is a fully site-based 6-month contract role. Fully site‑based roles This is a fully site‑based role.

As a Quality Control Expert on our Visp site, you will serve as the master bridge between global pharmaceutical clients, analytical laboratories, and Drug Product release. If you thrive on solving technical challenges, steering cross-functional teams, and making a tangible impact on global health—this is your platform to excel! ? ? ? ? ✨ Key Details: ? ? ? ? Location: Visp, Switzerland ? ? ? ? ? ? ? ?

Equipment Engineer Equipment Engineer - Small Devices Ensure the operational readiness and reliability of small manufacturing equipment at our BioAtrium facility in Visp, directly supporting the delivery of life-changing biopharmaceuticals. This is a fully site-based 6-month contract role. Fully site‑based roles This is a fully site‑based role.

Relocation assistance is available for eligible candidates and their families, if needed. Based in Basel, this role sits at the heart of Lonza-s Microbial manufacturing network, driving end-to-end supply planning to ensure reliable, efficient, and compliant delivery of products that support life-changing medicines. This is a fully site-based role.

Execute manufacturing activities in the Drug Product area following cGMP guidelines. Perform visual inspection of vials and provide technical support to the manufacturing team. Requires GMP experience and a structured, proactive approach.

The Process Excellence Specialist leads continuous improvement projects in Supply Chain. This role drives initiatives from opportunity identification through verified sustainment, utilizing Lean and structured problem-solving tools.

Laboratory Analyst in QC HPLC performs routine analysis of biopharmaceuticals using HPLC and capillary electrophoresis. Responsibilities include executing methods per SOP/GMP and supporting lab maintenance.

QC Analyst/Data Reviewer conducts routine biopharmaceutical analysis using HPLC and capillary electrophoresis. Responsibilities include reviewing QC data for accuracy and compliance with GMP and SOPs. A lab technician training or a relevant bachelor's degree is required.

Ref 2574676 | Date: 26 Août 2026 Logistic Specialist For our partner located in Visp, GI Life Sciences is looking for a : Logistics Specialist Start date : ASAP Temporary position End date : July 2027 Your mission : You will ensure the smooth execution of logistics and administrative activities related to inventory management.

Automation Engineer MES/DeltaV The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Senior Scientist QC manages GMP reference standard qualification protocols and reports for biotechnological materials. This role requires a Master's in Life Sciences, cGMP experience, and expertise in analytical chemistry/biology and QC software.

Associate Principal Scientist in Analytical Development. This hands-on role involves applying advanced analytical technologies, serving as an AD representative on pre-clinical teams, and acting as an SME for analytical methods. Requires a relevant degree and professional experience.

Ensure critical GMP processes are validated and maintained in compliance with global regulatory guidelines. Oversee validation activities for biotechnological manufacturing, manage CPV, and act as a QA point of contact for product transfer.