402 English-speaking jobs in Canton of Valais

Manage store operations, including inventory, ordering, and maintenance. Lead a team of 5, provide customer service, and ensure compliance with procedures and regulations.

Senior Cleanroom Hygiene & Contamination Control Specialist ensures GMP-compliant cleanroom environments and drives contamination control strategies. Leads hygiene projects, manages cleanroom performance qualifications, and investigates deviations. Requires a degree in a scientific discipline and experience in GMP-regulated environments.

Lead Expeditor to manage and coordinate expediting activities, ensuring On Time Delivery (OTD) performance and supplier performance tracking. Requires strong organizational and communication skills, problem-solving abilities, and experience in data analytics and reporting.

Manufacturing GMP Operative / Cleanroom Operator needed for a 6-month contract. Responsibilities include cleanroom cleaning, material disinfection, GMP documentation, and support of production activities. Requires at least 1 year of experience in a GMP-regulated environment and fluency in English or German.

Manage store operations, including inventory, ordering, and maintenance. Lead a team of 5, provide customer service, and ensure compliance with procedures and regulations.

Manage store operations, including inventory, maintenance, and team of 5. Ensure customer service and compliance with procedures and legislation. Requires a Federal VET Diploma in retail management and 10+ years of experience in retail management or a similar role, with experience in the food trade.

Lead and manage a team of Automation Engineers, ensuring alignment with operational priorities. Collaborate with Operations, MSAT, and Quality to deliver automation objectives. Manage a local Center of Excellence for MES and DCS Automation, contributing to standardization efforts. Provide expertise in DeltaV, Syncade, GMP lifecycle management, and biological manufacturing.

Senior QA Specialist ensures quality requirements for manufacturing processes and cGMP standards are met. Represents QA in project/tech transfer organizations and reviews/releases quality-related documents. Performs assessments for product changes, investigates deviations, and trains junior employees. Requires a degree in a related field, experience in the GMP regulated pharmaceutical industry, and strong communication skills.

Global Transformation Lead for Indirect Procurement will architect the 5-year aspiration plan for the Global Indirect Procurement organization. This role leads the Spend Optimization Project, addressing 800MCHF in spend across global categories. The individual will serve as a high-level interface between procurement, finance, and business leadership, ensuring strategic alignment with long-term execution plans.

As In Room Dining Host, you will deliver exceptional guest experiences while embodying Six Senses' vision and values. You will ensure efficient service, uphold sustainability practices, and contribute to creating memorable "Out of the Ordinary" moments.

Process Analytics & Operational Intelligence Expert will build analytics-ready datasets, analyze process trends, and develop dashboards to improve operational performance. Collaborate with manufacturing and process teams to translate data into actionable insights and support GMP deliverables.

Lead MES projects across all lifecycle phases, from requirement analysis to deployment. Maintain, optimize, and develop MES standards ensuring compliance and alignment with site and global guidelines. Ensure reliable operation and updating of MES systems, recognizing their impact on production processes and GMP-compliant documentation. Collaborate with Operations, QA, Automation, and IT/OT teams.

Lab Analytical Scientist to support analytical activities for clinical development and process validation stage products. Focus on method suitability assessment, validation, verification, and transfer in alignment with GMP ICH guidelines. Requires expertise in physical and chemical technologies.

Support day-to-day QC activities, perform laboratory activities under GxP conditions, and document data.

Senior Bioprocess Engineer needed for operational activities including tech transfer, material planning, and training. Leads interdisciplinary teams and guides activities for clinical and commercial manufacturing. Requires a Bachelor's, Master's, or PhD in a Life Science subject and significant experience in biomanufacturing. Excellent communication skills in English and/or German are essential.

Phys-chem Lab Analytical Scientist needed for 12-month contract (potential extension) in Visp, Switzerland. Supports analytical activities for clinical development products, focusing on method suitability assessment/validation/verification/transfer. Requires 5+ years of experience in Pharma industry/GMP, including change management and qualification activities. Bachelor's or Master's degree in a relevant field is required. Fluent English, German is a plus.

QA Raw Material Compliance Specialist manages Vendor Change Notifications (VCNs) ensuring compliance with internal quality systems and regulatory requirements. The role involves working across SAP, TrackWise, and document management systems.

The Batch Record Review Intern supports the Quality Assurance team by reviewing, verifying, and organizing electronic GMP manufacturing documentation. This role involves reviewing executed batch records, clarifying comments, and supporting deviation and investigation processes.

Supports the QA Supplier Management Team in managing Vendor Change Notifications (VCNs). Reviews, assesses, and coordinates the evaluation of VCNs, ensuring compliance with internal procedures and regulations.

QA Raw Material Compliance Specialist needed to support the management of Vendor Change Notifications (VCNs). Responsibilities include reviewing, assessing, and coordinating the evaluation of VCNs, ensuring compliance with internal procedures and regulatory expectations. Requires a Bachelor's or Master's degree in a relevant field, 5+ years of experience, and strong understanding of GMP regulations and change control processes.