103 centre de formationpour les cha 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, leveraging contamination control expertise to influence continuous improvement initiatives. Authors and approves GMP documentation, including SOPs, deviations, change controls, and risk assessments. Partners with cross-functional teams to identify risks, manage deviations, and strengthen contamination prevention control practices. Acts as a QA Microbial Contamination Control and cleaning SME in meetings, audits, and inspections.

Lead and shape a comprehensive contamination control strategy in a GMP-regulated bioconjugates environment. Drive cross-functional collaboration, leverage contamination control expertise, and influence continuous improvement initiatives.

Program Management Analyst will translate data into informative views to support data-driven action. The role involves updating reporting, providing SAP technical support, and collaborating with Finance on revenue reconciliation.

Associate Principal Scientist - Analytical Development will serve as the AD representative on pre-clinical project teams, coordinating with internal SMEs across all project phases. The role requires experience in protein analysis, physical-chemical methods, biochemical assays, and/or molecular biology techniques.

Leads a team in deviation investigation, ensuring timely closure and adherence to production schedules. Manages deviation lifecycles, reviews reports, and collaborates with stakeholders to improve processes. Provides supervision, training, and development for team members. Requires a Bachelor's degree in a Science/Engineering field and experience in cGMP regulated environments.

Team Lead Visual Inspection manages personnel, development, and daily production tasks. The role involves training, coaching, performance reviews, and collaborating with other team leaders. Experience as a production shift team leader and knowledge of Visual Inspection processes are required. Fluency in English is essential, German is advantageous.

Lead and develop a high-performing operations team, plan workloads, and ensure timely project delivery. Serve as the primary point of contact for stakeholders and support operational strategy development.

Senior QA Specialist for Contamination Prevention & Control (CPC) Environmental Monitoring (EM) team. Develops GMP-compliant EM reports, supports batch release reviews, and analyzes contamination control data. Requires a university degree in a relevant field, strong scientific background, and experience with GMP documentation and regulatory requirements.

Bioprocess Engineer to support clinical and commercial manufacturing of therapeutic proteins. Responsibilities include operational activities, process execution, and leading defined USP or DSP areas. Requires a Master's degree or equivalent experience in a Life Science field, knowledge of USP or DSP units, and GMP experience.

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.

The Associate Director, Asset Design and Innovation will lead the development and implementation of innovative manufacturing solutions, focusing on technological advancements and asset design.

Lead customer programs from technology transfer to GMP manufacturing, ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner and main point of contact for customers, fostering transparent communication and long-term collaboration.

Experienced Data Center Technician needed for freelance/contract work in Leuk Stadt, Switzerland. On-site support of mission-critical infrastructure. Responsibilities include hardware installations, cabling, server racking, troubleshooting, and documentation. Requires 2+ years of data center experience, strong cabling skills, and the ability to lift 50+ lbs.

Lead customer programs from technology transfer to GMP manufacturing, ensuring quality, timelines, and cost-effectiveness. Act as a trusted partner and main point of contact for customers, fostering transparent communication and long-term collaboration.

Senior Manager, Process Automation Lead drives process automation strategy, governance, and recipe development for capital growth projects and legacy asset improvements. Leads a team of consultants and contractors, ensuring alignment between process requirements and automation solutions.

Lead complex programs from contract signature to delivery in microbial drug substance manufacturing. Manage cross-functional teams, ensure on-time and on-budget delivery, and communicate with stakeholders. Bachelor's or Master's degree in a related field and multi-year experience in project or program management are required.

Sommelier and Room Attendant responsible for upholding Six Senses values and ensuring guest satisfaction. Duties include assisting guests, maintaining room cleanliness and supplies, and adhering to service standards.

Senior QA Specialist manages quality-related responsibilities for biopharmaceutical manufacturing processes, ensuring compliance with cGMP standards. Oversees QC, logistics, supply chain, and manufacturing activities. Represents QA in project and tech-transfer organizations. Reviews and releases quality documentation. Assesses product-related changes and supports investigations of customer complaints. Requires a degree in a relevant field, significant experience in biopharmaceutical manufacturing, and strong cGMP knowledge. Excellent communication skills and experience interacting with regulatory agencies are essential.

Provides QA support for GMP & Compliance, Cold-chain, supply chain, good warehousing practice, and Clean utilities. Oversees site and facilities focusing on shared utility systems and logistics areas. Reviews and assesses Change Requests, CAPAs, and SOPs. Supports audits, inspections, and represents the Quality function at meetings. Leads or supports local implementation of global Quality policies and standards.

Lab Analytical Scientist to support analytical activities for clinical development and process validation. Focus on method suitability assessment, validation, verification, and transfer. Requires expertise in physical and chemical technologies and pharmacopeia requirements. Full-time, on-site presence required.