109 marketing English-speaking jobs in Canton of Valais

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.

Cleaning Validation Expert needed for Large-Scale Mammalian facility in Visp. Develop and coordinate cleaning validation strategies, prepare documentation, and act as Subject Matter Expert for cleaning related matters. Master's or PhD in biotechnology, life sciences, or related disciplines required. Experience in biopharma cleaning and/or validation in a cGMP environment is essential.

Process Expert leads multi-functional teams for technology transfers, process implementation, and optimization of mammalian processes at manufacturing scale.

Manufacturing Line Specialist (Anlagemeister) ensures production of therapeutic proteins in a large-scale facility, adhering to cGMP guidelines. Responsibilities include equipment maintenance, troubleshooting, employee training, and cross-functional support. Requires a technical background and fluency in English. German is a plus.

Bioprocess Engineer will plan, execute, and oversee USP manufacturing campaigns, ensuring safety, quality, and on-time delivery. Responsibilities include process evaluation, troubleshooting, risk assessments, and document preparation. Requires a BSc or MSc in a relevant field or 7+ years of experience in USP operations. Experience with MES/DeltaV is advantageous.

This internship supports the global Master Data department in Visp. Assist with data analysis, SAP master data maintenance, and gathering feedback from Subject Matter Experts. Develop training materials and deliver training sessions.

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.

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.

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

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.

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.

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.

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.

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.

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.

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.