6 English-speaking jobs in Visp
Senior Program Manager Microbial - 80-100% (f/m/d)
- Lonza Group
- Visp
- July 22
Relocation assistance is available for eligible candidates and their families, if needed. The site in Visp, Switzerland is growing and we are currently looking for (Senior) Program Managers for our Microbial BU. In this role, you will be the Key interface between Sales and Operations in order to deliver and execute customer contracts.
DeltaV Automation Engineer 80-100% (m/f/d)
- Lonza Group
- Visp
- July 19
DeltaV Automation Engineer needed for planning and realization of electrical MSR readiness within budget and timelines. Ensures seamless operation of high-automated Biologics facilities equipped with DeltaV and MES systems. Requires experience in pharmaceutical or biotech industry, proficiency in SAP, COMOS, DeltaV, and MES Syncade.
MSAT Bioconjugates Process Expert (f/m/d) - 80% -100%
- Lonza Group
- Visp
- July 17
Process expert to deliver biopharma API manufacturing expertise, support process technology transfer, and lead process optimization. Requires a Master's degree or PhD in a related scientific discipline and significant industry experience in bioconjugation methodologies and biopharma manufacturing.
(Senior) Program Manager, Integrated Biologics 80 - 100%
- Lonza Group
- Visp
- July 17
Lead and deliver customer programs from technology transfer to GMP manufacturing, ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner for customers, fostering transparent communication and collaboration. Manage scope, timelines, and financials while aligning with strategic business goals.
Laboratory Technician QC Biochemistry (all genders)
- Lonza Group
- Visp
- July 16
Laboratory Technician to perform analytical protein analysis, including ELISA and qPCR, in compliance with GMP guidelines. Requires an apprenticeship as a Laboratory Technician, BTA or BSc in Biology, and experience with ELISA.
(Senior) Scientist (m/w/d) Quality Control, Environmental Monitoring
- Lonza AG
- Visp
- July 3
Evaluates complex monitoring data, improves processes, and supports compliance in a GMP-regulated environment. Conducts root-cause investigations, documents GMP activities, and creates/reviews documents. Requires a life sciences degree and 2+ years of relevant experience.
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