69 marketing English-speaking jobs in Visp

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.