109 marketing English-speaking jobs in Canton of Valais

PhD student to develop advanced social-AI models for behavior understanding in autism early screening, diagnosis, and monitoring. Focus on multi-behavior coordination models (face and body gestures, gaze, audio, semantics) with temporal interpretation.

Freelance Data Center Technicians provide on-demand support to global data centers. Responsibilities include hardware installation, troubleshooting, network management, and documentation. Expertise in data center equipment, software, and security protocols is required.

Freelance Data Center Technician needed for on-demand support of global data centers. Responsibilities include hardware installation, troubleshooting, network management, and documentation. Requires 3+ years of experience, expertise in Cisco/Juniper networking, and proficiency in Windows/Linux systems.

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.

Coordinate and support downstream production activities across various departments to ensure timely and compliant execution. Lead workforce planning, training, and performance management for DSP production support. Manage recruitment and onboarding of production personnel.

QA Project Manager will establish Quality Agreements, act as QA representative in project teams, and support customer audits. Requires a university degree in a relevant field and long-term GMP experience in the pharmaceutical industry.

Process Analytics & Operational Intelligence Expert will build analytics-ready datasets, analyze process trends, and develop dashboards to improve operational performance.

Lead MES projects across all lifecycle phases, from requirement analysis to deployment. Maintain and optimize MES standards, ensuring compliance and alignment with guidelines. Collaborate with Operations, QA, Automation, and IT/OT teams to ensure seamless system integration and high system availability.

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.

Laboratory Technician will conduct routine HPLC analysis of biopharmaceuticals, adhering to SOPs, GMP, and safety rules. Experience with HPLC and a GMP environment is preferred. Fluency in English or German is required.

Senior Bioprocess Engineer to manage operational activities, including tech transfer, material planning, and training. Lead interdisciplinary teams and guide 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.

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.

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).

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.

Drive growth for Lonza's Specialized Modalities platform across mainland Europe. Build customer relationships, develop new business opportunities, and deliver tailored solutions.