81 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.

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.

The CQV Engineer performs validation activities for equipment, facilities, and utilities, including URS, FAT/SAT, IQ/OQ/PQ. Responsibilities include preparing validation documentation, executing IQ/OQ/PQ, and writing reports. The role also involves identifying efficiencies in the validation program, applying lessons learned, and supporting the Engineering group with validation, requalification, and maintenance programs.

The CQV Engineer performs validation activities for equipment, facilities, and utilities, including URS, FAT/SAT, IQ/OQ/PQ. Responsibilities include preparing validation documentation, executing IQ/OQ/PQ, and writing reports. The role also involves identifying efficiencies in the validation program, applying lessons learned, and supporting the Engineering group with validation, requalification, and maintenance programs.

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.

Automation/Control Systems Engineer will plan and execute electrical MSR readiness, ensuring seamless operation of automated Biologics facilities. Experience with DeltaV, MES, SAP, COMOS, and GMP is required.

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.

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.

Team Lead Visual Inspection manages personnel, development, and daily production tasks. The role involves training, coaching, performance reviews, and collaborating with other team leaders. Experience as a production shift team leader and knowledge of Visual Inspection processes are required. Fluency in English is essential, German is advantageous.

Lead, Visual Inspection Operations manages personnel, development, and daily production tasks. The role involves training, coaching, performance reviews, and collaborating with other team leaders. Experience as a shift team leader in production and fluency in English are required.