81 English-speaking jobs in Visp

Leads, coaches, and develops employees in a pharmaceutical production environment. Responsible for daily tasks, training, performance reviews, and ensuring safety and GMP compliance. Requires past experience as a shift team leader in production and fluency in English.

As Team Lead Visual Inspection, you will manage and develop employees, oversee daily production tasks, and participate in investigations and improvement projects. You will ensure safety and GMP compliance, interpret and eliminate deviations, and participate in audits. Experience as a shift team leader in production and fluency in English are required.

As Team Lead Visual Inspection, you will manage and develop employees, oversee daily production tasks, and participate in investigations and improvement projects. You will ensure safety and GMP compliance, interpret deviations, and participate in audits. Experience as a shift team leader in production and fluency in English are required.

Project Leader in Analytics will establish and maintain customer relationships, prepare production campaigns, and process change requests. Requires a PhD or equivalent in Life Sciences and experience in a GMP environment. Excellent communication skills in English are required.

Design, build, and enhance SAP EWM solutions supporting warehouse and labeling operations. Act as an IT business partner, translating business needs into functional specifications. Configure and customize SAP EWM in line with global processes and governance. Provide third-level support for complex system incidents and problems.

As Team Lead Visual Inspection, you will manage and develop employees, oversee daily production tasks, and participate in investigations and improvement projects. You will ensure safety and GMP compliance, interpret and eliminate deviations, and participate in audits. Experience as a shift team leader in production and fluency in English are required.

QA Specialist for raw materials and consumables, ensuring documentation, data, and processes meet internal standards and regulatory requirements.

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

Electrical Instrumentation & Control Technician will plan and execute maintenance and calibration activities for electrical, measurement, and control systems. Troubleshooting, documentation, and collaboration with teams are key responsibilities.

The Head of OE & PMO leads the Operational Excellence and PMO agenda, driving business results aligned with the Dedicated to Excellence strategy. The role leads and develops a team of OE Business Partners and OE/PMO Managers, coaches the Mammalian Operations leadership team, and embeds Lean Six Sigma principles. Responsible for Hoshin planning, X‑Matrix deployment, Project Portfolio Management (PPM), and PMO governance, the role translates strategy into actionable operational excellence and innovation projects.

Intern supports material management and process-related activities in microbial cGMP manufacturing. Assists with material quality issues, single-use assembly design, and process documentation. Collaborates with cross-functional teams to ensure robust and compliant processes.

The Associate Director, Asset Design and Innovation will lead the development and implementation of innovative manufacturing solutions. This role will drive technological advancements and asset design to support strategic growth projects.

Senior MSAT Specialist will lead impurity risk assessments and develop control strategies for Small Molecules, ensuring compliance with ICH Q3D, Q3C, and Q9. This role requires strong analytical and communication skills, experience in GMP environments, and the ability to collaborate effectively across functions.

MES Expert to author and adapt MES/PCS recipes for drug product manufacturing. Responsible for defining MES recipe concepts, building GMP documents, providing front line support, and training end users. Requires experience in MES recipe authoring, preferably in Emerson Syncade, and process knowledge in sterile drug product manufacturing.

QA Specialist will support QA Operations teams, including Clean Utilities and Environmental Monitoring. Responsibilities include developing, implementing, and monitoring quality procedures to ensure compliance with GxP standards and regulations. The role requires experience in a regulated environment, GMP compliance expertise, and strong communication skills.

Leads and executes equipment cleaning validation activities, including authoring and reviewing protocols and reports for COP, CIP, USP, DSP, and buffer/media systems. Supports SOP lifecycle for cleaning validation and coordinates with cross-functional teams on new or modified cleaning processes.

Provides technical expertise and operational support for equipment cleaning validation activities. Leads and executes cleaning validation protocols and reports for various systems. Collaborates with cross-functional teams to ensure GMP compliance and regulatory readiness.

Lonza is seeking motivated individuals to support vaccine production at a new plant in Visp. Responsibilities include defining and setting up production processes, operating equipment, and ensuring compliance with SOPs and regulations. Candidates with experience in pharmaceutical production or relevant qualifications are encouraged to apply.

Manufacturing Specialist will perform upstream or downstream manufacturing activities following cGMP guidelines. Troubleshoot equipment, evaluate test results, and recommend solutions. Prepare and maintain documentation such as batch records and SOPs. Contribute to capital investment projects and equipment commissioning. Train manufacturing staff on equipment and standard operations.

Microbial Contamination Control Expert (w/m/d) will create and implement contamination prevention measures in accordance with cGMP guidelines. Responsibilities include updating and executing gap assessments, creating SOPs, and serving as a point of contact for contamination prevention.