71 English-speaking jobs in Visp

Manage material processes in module L to ensure timely availability for production. Collaborate with manufacturing and supply chain teams to optimize material use and meet production needs.

Senior Program Manager responsible for leading complex programs from contract signature to delivery. Manages cross-functional teams, ensures on-time and on-budget project completion, and acts as the customer advocate. Requires a Bachelor's or Master's degree in a relevant field, multi-year project management experience, and strong communication and leadership skills. Fluency in English is required, German is a plus.

Manages a team of 6x20k DSP production staff, overseeing safety, quality, and on-time delivery. Collaborates with the Head of DSP on production planning, problem-solving, and innovation projects. Responsible for shift team performance, safety culture, training, and long-term planning.

Perform analytical methods in QC biochemistry, including ELISA and qPCR, ensuring compliance with GMP and safety regulations. Support method implementation, validation, and transfer activities. Contribute to process improvement and daily laboratory operations.

Supply Chain Project Team E2E Lead will bridge the gap between clients and internal teams to ensure flawless operational execution. The role requires strong analytical abilities, presentation skills, and experience in supply chain management, ideally within Pharma or CDMO.

Design and develop end-to-end applications for digitalization and automation use cases. Build APIs, services, and user interfaces supporting scientific and operational workflows.

The Senior Manager - Process Automation Lead drives process automation strategy, governance, and recipe development for Global Engineering projects. The role leads a team of specialists and external resources, ensuring automation solutions align with manufacturing and process requirements.

Experienced MSAT EM Expert needed for Performance Qualification activities, validation projects, and technical investigations in a GMP-regulated environment.

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.

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.

Electrical Instrumentation & Control Technician will plan and execute maintenance and calibration activities for electrical, measurement, and control systems. Troubleshooting, documentation, and collaboration with teams are key responsibilities.

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.

Subject Matter Expert (SME) in environmental qualification, analytical testing, and product knowledge. Leads Environmental Monitoring (EM) performance qualifications (PQ) and ensures compliance with European GMP, ISO13485, and 21CFR820 standards.

Executes manufacturing activities in Drug Product according to cGMP guidelines. Ensures batch execution, evaluates test results, and resolves issues. Provides technical and procedural support to the manufacturing team. Responsible for production documentation and supports process investigations and CAPAs. Requires 2-4 years of experience in a GMP environment and fluency in English or German.

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.

The Global Transformation Lead for Indirect Procurement develops and executes 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 serves as a strategic interface between procurement, finance, and business leadership, ensuring alignment between strategic setup and execution plans.

CSV Engineer responsible for the validation of computerized systems on process engineering equipment and facilities. Prepares commissioning and validation documents, supervises deviations and changes, and coordinates CSV executions with internal and external groups. Requires a technical degree and significant experience in CSV within a regulated environment.

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.

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.