“Full-time on-site HVAC and production plant technician role at (COMPANY NAME) in Visp, Switzerland. Responsible for maintaining heating, ventilation, and production systems in a GMP-regulated biopharma environment with competitive salary and benefits.”
“Site-based Junior Laboratory Technician role in Visp for QC Spectroscopy at (COMPANY NAME). Requires lab experience, spectroscopy knowledge (IR/UV/NMR), and GMP familiarity. Full-time position with career growth in quality control and lab management.”
“Full-time laboratory technician role in Visp, Switzerland (12 Oct-31 Dec 2026) for mammalian analytical development. Executes bioanalytical assays (ELISA, Gyrolab, qPCR) to support bioprocess quality. Requires vocational training or BSc/MSc in Life Sciences, hands-on lab experience, and English fluency. Competitive hourly rate offered.”
“7-month Quality Control Specialist role in Visp (41h/week) for (COMPANY NAME)/Randstad. Requires Life Sciences Master's/PhD, GMP experience, LIMS/TrackWise knowledge, English fluency (German asset). Site-based with cross-functional collaboration in biopharmaceutical QC.”
“Full-time (80-100%) engineering role at (COMPANY NAME) (Visp) for Anlagen-, Projektingenieur BioAtrium. Requires mechanical/process engineering degree, GMP knowledge, and Pharma/Biotech experience. Focus on plant maintenance, project realization, and process optimization with competitive salary and benefits.”
“Temporary Associate Scientist QC role at (COMPANY NAME)'s Visp site for lab investigations and deviation management. Requires GMP experience, LIMS/CDS proficiency, and strong technical writing skills. Fully on-site with collaborative team environment. Focus on patient safety and product quality.”
“(COMPANY NAME) seeks a QC LabTech (80-100% role) in Visp, Switzerland, for HPLC analysis in biopharmaceuticals. Requires lab technician apprenticeship or BSc in Chemistry/Biochemistry, GMP experience preferred. Competitive salary, relocation assistance, and benefits included.”
“Project Planner role in Visp for (COMPANY NAME) to manage integrated master schedules for large-scale pharmaceutical capital projects. Requires 5-10 years of experience, proficiency in Primavera P6 and Microsoft Project, and on-site presence. Bachelor's degree in Engineering or related field preferred.”
