122 English-speaking jobs in Canton of Valais

Temporary Collection Manager role overseeing commercial performance and growth of the regional property portfolio. Responsibilities include market analysis, pricing strategy, owner relationship management, and property sourcing.

Lead CQV activities for large-scale CAPEX projects in a GMP environment. Develop strategies, manage resources, and ensure regulatory compliance across project lifecycles. Requires a Master's degree and experience in Pharma/Biotech.

DeltaV Automation Engineer will plan and execute electrical MSR readiness, ensuring seamless operation of Biologics facilities. Experience in pharmaceutical or biotech plant operation and maintenance is required. Proficiency in DeltaV, MES, SAP, and COMOS is highly desirable.

Junior Biotechnology Production Operator for a temporary assignment in a biopharmaceutical environment. Responsibilities include performing production operations under cGMP, ensuring traceability, and following HSE requirements. Requires a science background and initial manufacturing experience.

CQV Manager leads and manages Commissioning, Qualification & Validation activities for large-scale CAPEX projects in a GMP environment. Requires a Master's degree and proven experience leading CQV on complex projects.

Lead DSP manufacturing campaigns, providing technical expertise in chromatography, filtration, and UF/DF. Drive operational excellence, manage teams, and ensure cGMP compliance. Requires a relevant degree and 5+ years in biotechnology.

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, while supporting the teppanyaki and hot Asian kitchen. Requires experience in Japanese/Asian cuisine and fluent English.

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.

Ensure compliance and data integrity by performing rigorous batch record reviews. Analyze electronic and paper records in MES, SAP, and LIMS environments, aligning with ALCOA+ and GDP principles.

Batch Record Reviewer ensures compliance and data integrity for life-saving medicines. Responsibilities include rigorous review of electronic and paper records within MES, SAP, and LIMS environments. Requires a Life Sciences degree and GMP 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.

Design and implement Emerson DeltaV automation solutions for biotech CAPEX projects. Requires experience in configuring DeltaV systems within regulated environments, knowledge of GxP/GAMP5, and fluency in German and/or English.

Develop international sales activities to meet revenue objectives, managing key client relationships and sales pipelines. Ensure adherence to Six Senses values, sustainability directives, and drive team performance.

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.

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.

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.