82 switzerland English-speaking jobs in Visp

At Lonza, we offer an outstanding opportunity for a CSV Engineer in Switzerland.

Location: the actual location of this job is in Visp, Switzerland.

Location: The actual location of this job is in Visp, Switzerland.

The actual location of this job is in Visp, Switzerland.

The actual location of this job is in Visp, Switzerland.

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.

Warehouse Operator needed to manage the movement, storage, and distribution of materials and products. Responsibilities include tracking shipments, inspecting items for quality, and ensuring accurate records. Must have strong attention to detail and the ability to read and interpret production schedules and orders.

Physchem Lab Analytical Scientist supports analytical activities for clinical development products. Focus on method suitability assessment/validation/verification/transfer per GMP, ICH guidelines, and company quality system. Requires 5+ years of pharma industry/GMP experience, Bachelor's degree, and fluency in English. German is a plus.

Freelance/temporary Biotechnologist needed for a project in Visp. Executes general cleaning in a clean room environment, disinfects materials, and compiles GMP documentation. Requires solid GMP experience, fluency in English or German, and strong team orientation.

Lab Analytical Scientist needed to support analytical activities for clinical development and process validation. Focus on method suitability assessment, validation, verification, and transfer. Requires expertise in physical and chemical technologies, pharmacopeia requirements, and global alignment. Full-time, on-site presence required.

QA Raw Material Compliance Specialist will support the management of Vendor Change Notifications (VCNs) ensuring compliant and controlled implementation. Responsibilities include reviewing, assessing, and coordinating VCNs, completing impact assessments, and managing VCNs according to GMP requirements.

Biotechnologist to support manufacturing operations in a clean room environment. Ensures safe, clean, and compliant production of liquid and freeze-dried drug forms. Collaborates with the manufacturing team to meet production needs while adhering to GMP standards.

Project Engineer needed for freelance/temporary employment in Visp. Define technical requirements, manage project roadmaps, and ensure GMP compliance. Experience in biopharmaceutical manufacturing, project management, and CQV activities required.

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.

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.

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.

Lead Expeditor needed to ensure timely delivery of materials and maintain efficient procurement processes. Coordinate with suppliers, manage reporting systems, and support internal stakeholders. Requires strong organizational, communication, and problem-solving skills. Proficiency in Microsoft Office, data analytics, and reporting is essential. Fluency in English is required. Relevant experience in a similar role, with CAPEX experience preferred. Must be able to work both on-site and remotely.

Lead and manage a team of Automation Engineers, ensuring alignment with operational priorities. Collaborate with Operations, MSAT, and Quality to deliver automation objectives. Manage a local Center of Excellence for MES and DCS Automation, contributing to standardization efforts. Provide expertise in DeltaV, Syncade, GMP lifecycle management, and biological manufacturing.

Coordinate and support downstream production activities across various departments to ensure timely and compliant execution. Lead workforce planning, training, and performance management for DSP production support. Manage recruitment and onboarding of production personnel.

Lead MES projects across all lifecycle phases, from requirement analysis to deployment. Maintain and optimize MES standards, ensuring compliance and alignment with guidelines. Collaborate with Operations, QA, Automation, and IT/OT teams to ensure seamless system integration and high system availability.