69 marketing English-speaking jobs in Visp

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.

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.

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.

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.

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.

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.

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.

Manufacturing Specialist to support project setup and routine vaccine production. Responsibilities include process definition, qualification, execution of manufacturing activities, and documentation. Requires a chemical/biopharmaceutical education or equivalent experience and knowledge of biotechnological processes. Fluency in English is required.

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.

Senior QA Specialist will provide quality assurance oversight for site and facilities, focusing on shared utility systems and logistics areas. Responsibilities include providing QA support, leading deviation review boards, and reviewing change requests and CAPAs.

Biotechnologist needed for production in Visp, Switzerland. Requires chemical/biopharmaceutical education and experience in pharmaceutical production. Must be safety-conscious, knowledgeable in process engineering, and fluent in English. German language skills are advantageous. Willingness to work shifts is required.

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

As a Vorsorge- und Finanzberatende, you will cultivate existing client relationships, acquire new clients, and provide comprehensive financial and retirement planning advice. You will develop and sell tailored solutions in retirement planning and asset building while representing the company in your sales area.

Manufacturing Specialist will execute production steps, interpret deviations, and support training within a cGMP environment. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.

Biotechnologist with a background in chemical or biopharmaceutical sciences needed for production functions. Experience in pharmaceutical production and a safety-conscious work style are required. Fluent English, German is a plus.

Senior Operator/Biotechnologist supports production in a biopharmaceutical facility. Responsibilities include executing production steps, recognizing deviations, and training new team members. Requires a chemical/biopharmaceutical education, experience in pharmaceutical production, and fluency in English. German language skills are advantageous.

Develop and maintain commissioning and qualification documents for new plants. Supervise deviations, manage changes, and implement CAPAs. Coordinate efforts between internal teams and external service providers.

DeltaV Automation Engineer needed for planning and realization of electrical MSR readiness within budget and timelines. Ensures seamless operation of high-automated Biologics facilities equipped with DeltaV and MES systems. Manages GMP-compliant activities, including testing, documentation, and change management. Collaborates with cross-functional teams to refine internal procedures and achieve optimized workflows.