106 English-speaking jobs in Canton of Valais

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 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.

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.

Maintenance Specialist performs routine maintenance and renewal on mechanical equipment across multiple hydroelectric power plants. Requires a CFC in polymécanicien, mechanic, or equivalent, plus experience troubleshooting industrial mechanical equipment.

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.

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.

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.

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.

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.

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.

Oversee a kitchen section, preparing authentic Peruvian dishes like ceviche and lomo saltado. Manage quality, portion control, and hygiene while supervising junior staff. Requires culinary qualification and 2-3 years of Chef de Partie experience.

EI&C PI Engineer to administer, maintain, and optimize PI Data Archive systems. Responsibilities include configuring PI AF, developing analytics, and integrating PI with manufacturing systems like DeltaV and PLCs. Requires experience with PI SDK and GxP compliance.

Senior QA Specialist provides quality oversight for facility and cleanroom qualification. Responsibilities include environmental monitoring, investigating deviations, and supporting CAPAs within GMP environments. Requires a relevant degree and strong microbiological expertise.

QA Specialist supports contamination prevention and control for a global CMO. Responsibilities include facility and utility qualification, environmental monitoring, and ensuring compliance with regulatory standards. Requires a relevant scientific degree and GMP experience.

QA Logistics Specialist ensures material incoming verification and alignment with regulatory requirements. Responsibilities include managing material qualification, maintaining raw material data in LIMS, and ensuring GMP compliance. Requires a relevant Bachelor's degree and knowledge of quality systems.

Maintain high standards of cleanliness in staff accommodation, including bedrooms, bathrooms, and common areas. Prepare rooms for new arrivals and conduct inspections. Report maintenance issues and follow safety standards.

The Upstream Team Lead provides technical leadership and manufacturing support for USP operations, managing Bioprocess Engineers. This role oversees campaign execution, ensures cGMP compliance, and drives operational excellence.

Primary Teaching Assistant needed for Winter Term 2027. Support pupil learning, development, and wellbeing across the Primary School. Requires experience with primary aged children.

Automation Engineer to design, develop, and implement Emerson DeltaV solutions for pharmaceutical and biotech CAPEX projects. Requires experience with DeltaV, GMP, GAMP, and data integrity standards.