402 English-speaking jobs in Canton of Valais

Leads and shapes a comprehensive contamination control strategy within a GMP-regulated bioconjugates environment, ensuring end-to-end compliance across manufacturing facilities. Drives cross-functional collaboration, manages risk assessments, change requests, deviations, investigations, and CAPAs. Authors and approves GMP documentation, including SOPs, deviations, change controls, and risk assessments. Partners with cross-functional teams to identify risks, drive deviation management, and strengthen contamination prevention control practices. Acts as a QA Microbial Contamination Control and cleaning SME in meetings, audits, and inspections. Reviews and approves routine cleaning-relevant documents and finalizes records like SOPs, MBRs, Material Specifications, Deviations, Change Requests, Effectiveness Checks, Testing Protocols & Reports. Identifies emerging QA relevant topics and communicates with stakeholders, working on their development into new or existing Quality and Compliance strategies and/or standards. Supports continuous improvement programs to establish effective Quality Contamination Control.

Experienced Process Engineer needed for a 5-month contract supporting a pharmaceutical project in Visp, Switzerland. Responsibilities include process design documentation, calculations, and ensuring compliance with GMP standards. Requires expertise in pharmaceutical production processes, equipment sizing, and multidisciplinary collaboration. German language skills are preferred.

Full-time B2B Logistics & Dealer Service Intern supporting North American Retail Partners. Responsibilities include order management, customer service, process improvement, and utilizing technology to enhance efficiency.

Central Hygiene Project Manager will ensure the implementation and continuous improvement of hygiene standards at the Visp site. The role involves acting as a key link between departments, leading hygiene projects, and managing Cleanroom Performance Qualifications (PQs).

The Mont Cervin Palace seeks a steward for the summer 2026 season. Responsibilities include washing dishes, maintaining kitchen cleanliness, assisting with deliveries, and supporting kitchen staff.

Execute construction, installation, and maintenance of fiber optic networks. Install fiber optic cables, prepare cable ends and junctions, perform quality measurements, and fill out exit vouchers.

Intern to support QA documentation, ensuring cGMP compliance in manufacturing activities. Reviews Batch Records, analyzes data, and assists with deviations and investigations. Requires a degree in a relevant field and proficiency in English.

Intern QC Lab Associate will carry out routine analysis, contribute to method implementation and validation, and support laboratory maintenance. Requires experience in analytical lab work and fluency in German or English.

The Material Management Analyst supports the Material Management Head in coordinating the MRP team and ensuring alignment on key priorities and processes. This role manages the raw material portfolio, executes material-related projects, and provides expertise in the management of specialized material categories. The analyst also participates in supply chain development initiatives and supports the Head of Supply Chain with reporting and analysis.

MSAT Data Manager (f/m/d) will extract, structure, and curate manufacturing data to support data-driven decisions. Responsibilities include preparing process data for investigations, developing dashboards, and performing statistical analysis to evaluate process performance. The ideal candidate will have experience in biopharma manufacturing, data analytics, or a regulated environment and strong data handling and analysis skills.

The EMEA Associate Director of Business Development will drive growth for Lonza's Specialized Modalities platform. This role involves building customer relationships, developing new business opportunities, and collaborating with internal teams to deliver tailored solutions.

Senior Engineer will ensure the reliable and compliant startup of a new fill-and-finish facility. Responsibilities include overseeing qualification, validation, and handover of CAPEX projects, establishing technical systems for maintenance and performance optimization, and leading projects within a matrix structure. Requires a degree in Engineering, Pharmaceutical Technology, Biotechnology, or a related field, and extensive experience in Pharma Operations Engineering, specifically aseptic Fill & Finish processes and complex equipment.

The MES Expert configures, maintains, and optimizes the Manufacturing Execution System (MES) for the VIVA2 project. Responsibilities include developing recipe structures, resolving MES discrepancies, providing training, and overseeing change control processes. The ideal candidate has a degree in Engineering, Life Sciences, or a relevant apprenticeship, with experience in GMP environments and pharmaceutical production. Expertise in MES platforms and DeltaV is required.

QC Analyst Microbiology to perform routine microbiological testing in a GMP laboratory environment. Responsibilities include bioburden, endotoxin, water, and environmental testing using aseptic techniques. Must have experience in microbiology laboratory testing within a GMP environment and be able to work rotating shifts.

Cleaning Validation Expert needed for Large-Scale Mammalian facility in Visp. Develop and coordinate cleaning validation strategies, prepare documentation, and review cleaning-related documents.

Provides support for material management in microbial cGMP manufacturing processes. Assists with material quality issues, single use assembly design and qualification, and process troubleshooting. Collaborates with cross-functional teams to ensure robust and compliant processes. Requires a Bachelor's or Master's degree in a relevant scientific discipline and strong interest in microbial manufacturing.

Neuropsychologist at 70% conducts assessments and neuropsychological treatments for patients with neurological conditions. Collaborates with physicians and the interdisciplinary team. Requires clinical experience in neuropsychology and a FSP or EAN title.

Own contamination control strategy within facilities, equipment, and processes. Lead technical expertise on hygiene, microbiological QC, and deviations. Ensure hygienic integrity across the product lifecycle. Develop and improve hygiene concepts and microbial control strategies. Represent contamination control in projects, audits, and cross-functional forums.

CSV Engineer responsible for the validation of computerized systems on process engineering equipment and facilities. Prepares commissioning and validation documents, supervises deviations and changes, and coordinates CSV executions with internal and external groups. Requires a technical degree and significant experience in CSV within a regulated environment.

Manufacturing Specialist supports production in compliance with safety regulations and cGMP. Executes production steps, records data, and assists with training. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.