7 English-speaking jobs in Visp

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.