15 English-speaking jobs in Canton of Valais

DeltaV Automation Engineer to plan and realize electrical MSR readiness for high-automated Biologics facilities. Requires experience in Electrical/System Engineering, DeltaV, and GMP compliance.

Quality Control Expert responsible for Drug Product QC, Method Validation, and Batch Release. This role serves as the bridge between clients, labs, and release, requiring GMP compliance and lab coordination.

Production Engineer for a 6-month contract role, ensuring operational readiness of small manufacturing equipment. Responsibilities include equipment lifecycle management, maintenance, and serving as SME on CAPEX projects. Requires 10+ years of engineering experience, with 3+ in cGMP pharma/biotech.

Equipment Engineer for small devices supporting biopharmaceutical production. Drive equipment lifecycle management, maintenance, and serve as SME on CAPEX projects. Requires 10+ years of engineering experience, 3+ in cGMP pharma/biotech.

Quality Control Specialist for a 7-month assignment. Drive operational excellence, ensure GMP compliance, and coordinate daily QC activities. Requires Master’s/PhD in Life Sciences and experience in GMP environments.

Drive Automation Procurement strategy globally, owning high-value negotiations with OEMs. Lead CAPEX projects, optimize TCO, and manage supplier performance in pharmaceutical manufacturing. Requires 10 years of procurement experience.

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.

Finance Collaborator role requiring CFC employee or equivalent with 1-2 years of accounting experience. Responsibilities include invoice posting, payment initiation, general ledger tasks, and monthly reporting. Fluent English is required.

Assistant Housekeeping Manager assists in managing, training, and motivating the housekeeping team. Responsibilities include monitoring cleanliness standards, conducting inspections, handling guest complaints, and managing supplies and schedules.

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.

This role coordinates Cold Chain projects, supporting the design and implementation of temperature-controlled supply chain solutions. Responsibilities include managing documentation, monitoring progress, and ensuring compliance with regulatory and quality requirements.

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.

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