14 English-speaking jobs in Visp

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.

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.

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.

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.

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.

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.

Leads operational excellence and project management across Microbial Operations, driving performance, innovation, and scalability. Executes operational excellence strategy, implements Lean Six Sigma methodologies, and manages project portfolio. Collaborates with senior leadership to align priorities and execute initiatives.