For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Bioprocess Engineer.General Information:Start date: 01.02.2026Duration: until 30.11.2026Workplace: VispWorkload: 100%Working hours: StandardOur client’s site in Visp, Switzerland is growing and for their Biologics organization, we are seeking experienced Bioprocess Engineers.Tasks & Responsibilities:Correct execution of production campaigns in
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Scientist - QC Microbiology Lead.General Information:Start date: 01.12.2025Duration: until 31.08.2026Workplace: VispWorkload: 100%Remote/Home Office: possible, max 2 days, 100 % on-site preferredWorking hours: StandardTasks & Responsibilities:Technical representation of the QC Microbiology department internally and at customer
For one of our clients, a world leader in the CDMO industry and biotechnology, we are currently looking for a Scientist - QC Microbiology Lead.General Information:Start date: 01.12.2025Duration: until 31.08.2026Workplace: VispWorkload: 100%Remote/Home Office: possible, max 2 days, 100 % on-site preferredWorking hours: StandardTasks & Responsibilities:Technical representation of the QC Microbiology department internally and at customer
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
For Lonza AG in Visp, we are seeking an Administrative Assistant 100%Key Responsibilities:Provide essential administrative services and support to managementTrack, compile, and manage information of interestPrepare various administrative reportsHandle all correspondence (reading and answering)Manage sensitive and confidential information with discretion
For Lonza AG in Visp, we are seeking an Administrative Assistant 100%Key Responsibilities:Provide essential administrative services and support to managementTrack, compile, and manage information of interestPrepare various administrative reportsHandle all correspondence (reading and answering)Manage sensitive and confidential information with discretion
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