71 English-speaking jobs in Visp

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.

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.

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.

Provides site support as part of the QA supplier management team. Reviews, evaluates, and coordinates supplier change notifications, ensuring compliance and timely implementation.

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.

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.

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.

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.

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.

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.

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.

Senior QA Specialist to join a multifunctional team in Bioconjugates Business unit. Will support the establishment and maintenance of quality management & compliance processes. Responsibilities include coordinating QA interests during project phases, reviewing and releasing records, and managing stakeholder needs. Requires a degree in Biotechnology/Biochemistry or related field, significant experience in biopharmaceutical manufacturing, and strong cGMP knowledge.

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.

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.

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.

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.

MES Expert to author and adapt MES/PCS recipes for drug product manufacturing. Responsible for defining MES recipe concepts, building GMP documents, providing front line support, and training end users. Requires experience in MES recipe authoring, preferably in Emerson Syncade, and process knowledge in sterile drug product manufacturing.