69 marketing English-speaking jobs in Visp

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.

QA Raw Material Compliance Specialist ensures raw material quality and compliance by managing Vendor Change Notifications (VCNs). This role involves reviewing, assessing, and coordinating VCN evaluations, conducting impact assessments, and tracking VCNs to ensure adherence to procedures and regulations.

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.

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.

Experienced SAP EWM Functional Consultant needed for pharmaceutical project in Switzerland. Lead and support implementations, rollouts, and enhancements. Configure and optimize SAP EWM processes for pharma operations. Collaborate with international teams and ensure compliance with industry standards.

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.

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.

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.

Senior QA Specialist ensures quality requirements for manufacturing processes and cGMP standards are met. Represents QA in project/tech transfer organizations and reviews/releases quality-related documents. Performs assessments for product changes, investigates deviations, and trains junior employees. Requires a degree in a related field, experience in the GMP regulated pharmaceutical industry, and strong communication skills.

Global Transformation Lead for Indirect Procurement will architect the 5-year aspiration plan for the Global Indirect Procurement organization. This role leads the Spend Optimization Project, addressing 800MCHF in spend across global categories. The individual will serve as a high-level interface between procurement, finance, and business leadership, ensuring strategic alignment with long-term execution plans.

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.

QA Project Manager will establish Quality Agreements, act as QA representative in project teams, and support customer audits. Requires a university degree in a relevant field and long-term GMP experience in the pharmaceutical industry.

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.

The Batch Record Review Intern supports the Quality Assurance team by reviewing, verifying, and organizing electronic GMP manufacturing documentation. This role involves reviewing executed batch records, clarifying comments, and supporting deviation and investigation processes.

Process Analytics & Operational Intelligence Expert will build analytics-ready datasets, analyze process trends, and develop dashboards to improve operational performance.

Laboratory Technician will conduct routine HPLC analysis of biopharmaceuticals, adhering to SOPs, GMP, and safety rules. Experience with HPLC and a GMP environment is preferred. Fluency in English or German is required.