25 English-speaking jobs in Visp

Senior Scientist QC strengthens quality and compliance across the QC organization. Responsibilities include assessing GMP processes, leading deviation investigations, and supporting regulatory inspections. Requires a relevant advanced degree or extensive experience.

Implement, optimize, and support MES and Emerson DeltaV systems in biopharmaceutical manufacturing. Design control strategies, troubleshoot issues, and maintain GMP documentation. Requires experience in regulated environments.

MSAT Bioconjugates Process Expert responsible for supervising and managing bioconjugate processes. This role involves cross-departmental networking, process troubleshooting, and owning program life cycle management. Requires a Master's or PhD in a relevant scientific field.

Lead GMP deviation investigations for manufacturing and operational events. Conduct root cause analysis, impact assessments, and define CAPAs in a biopharmaceutical environment. Requires experience in GMP-regulated manufacturing.

Act as the QC Project Lead for customer programs, aligning QC activities with project objectives and customer expectations in a GMP-regulated environment. Coordinate analytical activities and manage risks across cross-functional teams.

Senior Lab Technician executes experimental work and manages lab operations. Requires a life science degree and experience in CHO cell culture, IgG purification, and analytical methods. Fluent English is required.

Senior QA Specialist for Analytics ensures quality oversight on GMP-relevant activities in QC and AD. Responsibilities include reviewing SOPs, analytical methods, and ensuring compliance with regulations. Requires a degree in Life Sciences and pharmaceutical industry experience.

Intern Cleaning BioProcess Engineer supports GMP manufacturing operations by assisting with cleaning validation of large-scale bioreactors and tanks. Responsibilities include documentation control and process improvement.

Senior SAP EWM Specialist supports global warehouse operations in a GMP/GxP environment. Responsibilities include designing, building, and enhancing SAP EWM solutions, acting as an IT business partner, and providing third-level support. Requires SAP EWM experience.

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.

Lead the application of AI/ML and data science to solve scientific and operational challenges. Design predictive models and drive innovation across Data Science & Modelling initiatives. Requires a PhD and industry experience in data science.

MSAT Principle Scientist to own and improve manufacturing cleaning processes and equipment cleaning strategies. Develop compliant cleaning concepts and lead CIP/COP improvement initiatives in a GMP-regulated environment. Requires MSc or PhD in a relevant science.

Senior Scientist in Quality Control and Environmental Monitoring evaluates complex data and improves processes in a GMP-regulated environment. Responsibilities include data collection, leading investigations, and ensuring compliance. A life sciences degree and two years of relevant GMP experience are required.

MSAT Expert for Material Management and Single-Use Systems. Act as SME for Raw Materials and Single-Use Systems, leading risk assessments and driving investigations, CAPAs, and change controls in GMP compliance.

Lead procurement activities for assigned portfolios, ensuring supply continuity and cost competitiveness. Manage supplier relationships, drive SRM initiatives, and oversee vendor performance. Requires SCM/Procurement experience and SAP MM knowledge.

Operations Support Specialist role involving raw material management, dispensing, and processing in a large-scale mammalian facility. Tasks include material transport, deviation elimination, and executing production steps under cGMP. Fluent English is required.

Senior QA Specialist supporting Infrastructure and Logistics at the Visp site. Responsibilities include QA oversight for utilities and logistics, managing deviations, and ensuring compliance with GMP and regulatory standards.

Senior Strategic Buyer manages a 50m CHF annual spend, ensuring supply for life-saving medicines. Responsibilities include negotiation, supplier performance, and mentoring. Requires a Business/Supply Chain degree and procurement experience.

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. Manages GMP-compliant activities, including testing, documentation, and change management. Collaborates with cross-functional teams to refine internal procedures and achieve optimized workflows.

Senior Program Manager for Integrated Biologics leads customer programs from contract to GMP delivery. This role requires leading cross-functional teams, managing scope and timelines, and ensuring quality in pharma or CDMO settings.