101 English-speaking jobs in Canton of Valais

Postdoctoral position to investigate shared autonomy for assistive robots in real-world home support. The role involves developing autonomy methods, system integration, and conducting rigorous evaluations with participants.

Asian Specialty Chef for a 5-star Alpine resort. Responsibilities include preparing sushi, sashimi, and nigiri, and supporting the teppanyaki and hot Asian kitchen. Requires experience in Japanese/Asian cuisine and fluent English.

Electrical Design Engineer responsible for designing and developing electrical systems in industrial environments. Key duties include designing infrastructure, power distribution networks, and UPS systems while ensuring compliance with standards. Requires an engineering degree and 4-10 years of relevant experience.

Postdoctoral position in embodied AI to investigate autonomous robots learning and adapting in clinical and pharmaceutical labs. Focus on robot learning, human-robot interaction, and neuro-symbolic control. PhD in related field required.

0 Batch Record Reviewer Batch Record Reviewer Are you looking to make a direct impact on the delivery of life-saving medicines? Join our dynamic Quality Assurance team in Visp as a Batch Record Reviewer, where you will ensure flawless compliance, data integrity, and operational excellence across critical production projects. This is a fully site‑based role.

Ensure compliance and data integrity by performing rigorous batch record reviews for life-saving medicines. Analyze electronic and paper records within MES, SAP, and LIMS environments, adhering to ALCOA and GDP principles.

Design and implement Emerson DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience.

Design and implement Emerson DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience in regulated environments.

Design and implement DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience in regulated environments.

Design and implement DeltaV automation solutions for biotech CAPEX projects. Configure control modules, graphics, and interfaces while developing GxP-compliant documentation. Requires engineering degree and DeltaV experience in regulated environments.

EI&C PI Engineer needed for a project. Responsibilities include administering PI Data Archive, configuring PI AF, developing analytics, and integrating PI with manufacturing systems like DeltaV and PLCs. Requires experience with PI SDK, SQL, and GxP compliance.

Senior QA Specialist for a project role. Responsibilities include quality oversight for facility qualification, environmental monitoring, and leading investigations. Requires a degree in a life science and GMP experience.

Lead a multidisciplinary team in biologics manufacturing as Associate Director, Manufacturing DSP. Drive operational excellence, ensure production readiness, and manage complex manufacturing challenges within a GMP-regulated environment.

Process Validation Specialist develops validation strategies and executes protocols for commercial manufacturing. This role requires a PhD or Master's in a relevant science, GMP experience, and strong analytical skills.

Senior QA Specialist for QA Projects defines quality requirements for biopharmaceutical manufacturing processes and cGMP standards. This role owns quality responsibilities, reviews critical records, and ensures compliance in cross-functional teams.

DSP Bioprocess Engineer responsible for planning, executing, and monitoring commercial and clinical manufacturing campaigns in Downstream Processing. Acts as manufacturing subject matter expert ensuring cGMP compliance and leading process improvements.

QA Logistic Specialist ensures pharmaceutical quality and compliance across global supply chains. Responsibilities include verifying incoming materials, overseeing material qualification, and managing quality alerts under GMP standards. Requires a relevant degree and knowledge of quality systems like SAP and LIMS.

Experienced EI&C Software Application Engineer needed to support automation and manufacturing software in a regulated environment. Develop, configure, and maintain applications using VBA, PowerShell, C#, and SQL. Requires IT/OT integration and GMP/GxP compliance.

Experienced MES System Engineer needed to support manufacturing systems in a GMP-regulated pharmaceutical/biotech environment. Responsibilities include maintaining MES, providing technical support, and ensuring GxP compliance. Requires relevant technical background and MES platform experience.

Leads technical transfer activities, including setup and implementation of sterile GMP DP manufacturing processes. Manages drug product transfers from clinical to commercial launch, ensuring cGMP compliance.