71 English-speaking jobs in Visp

Bioprocess Engineer needed for Upstream or Downstream Processing. Master's degree or equivalent experience in a Life Science field required. Knowledge of bioreactors or chromatography units and GMP experience necessary.

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

Bioprocess Engineer needed for Upstream Processing, Downstream Processing, or BioConjugate Manufacturing. Master's Degree or equivalent experience in a Life Science field required. Knowledge of USP or DSP units and GMP experience necessary.

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.

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.

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.

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.

Internship supporting the Global Master Data team in Visp. Assist with data analysis, SAP Master Data maintenance, and gathering feedback from Subject Matter Experts.

Own defined areas within the site Contamination Control Strategy, ensuring a sustained microbial state of control across facilities, equipment, processes, and supporting systems. Act as the technical lead for contamination control, hygiene, and microbiological QC topics. Provide visible shopfloor presence, hands-on technical support, and leadership on contamination control topics. Develop and improve hygiene concepts, gowning expectations, aseptic behavior, microbial hold times, and bioburden control strategies. Represent CCS and microbiological quality topics in projects, audits, regulatory inspections, and cross-functional governance forums. Drive continuous improvement, KPI delivery, training, and technical guidance.

Proclinical seeks a Project Buyer to execute operational procurement activities for capital expenditure (Capex) projects. This role involves requisition, purchase order creation, supplier coordination, and compliance with procurement processes.

The EHS Manager drives the implementation and improvement of Environmental, Occupational Health, and Safety programs in collaboration with manufacturing facilities. This role serves as the primary EHS contact for Large Scale Plants in Visp, ensuring safe, compliant, and sustainable chemical manufacturing.

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.

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 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 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.

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.

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.

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.