10 English-speaking jobs in Visp

QA Manager in QA Analytics ensures QC processes comply with GxP, data integrity, and regulatory standards. This role involves representing QA in cross-functional teams, reviewing QC documents, and driving CAPA items.

DSP Bioprocess Engineer responsible for planning, executing, and monitoring commercial and clinical manufacturing campaigns. Acts as manufacturing subject matter expert, ensuring cGMP compliance and driving process improvements. Requires expertise in biopharmaceutical manufacturing and quality systems.

Execute operational activities in Upstream, Downstream, or BMS processing for a large-scale mammalian facility. Responsibilities include batch execution, troubleshooting, deviation management, and supporting capital investment projects. Requires a relevant degree and knowledge of biotechnological processes.

Associate Director Manufacturing Bioconjugates leads new commercial production lines. This role oversees manufacturing performance in quality, output, and safety, leading a multidisciplinary team. Requires a degree in a relevant field and 5+ years in chemical or biotech manufacturing.

Design, build, and operate production-ready data pipelines integrating operational data from sources like MES and PI Historian. Requires strong SQL, ETL/ELT experience, and knowledge of manufacturing data environments.

Operator/Biotechnologist contributes to biopharmaceutical product manufacture, ensuring cGMP compliance. Responsibilities include executing production operations, investigating deviations, and maintaining accurate records. Requires education in life sciences and experience in regulated manufacturing.

Experienced Chemist/Chemical Engineer needed for Small Molecule Lead Chemist role focusing on DSP and preparative chromatography. Drive DSP technology improvement, lead process development, and support strategic growth. PhD required.

Senior Scientist in Quality Control and Environmental Monitoring evaluates complex data in a GMP environment. Responsibilities include leading investigations, improving monitoring processes, and ensuring compliance. Requires a life sciences degree and relevant experience.

KPC International seeks experienced Commissioning, Qualification, and Validation professionals for pharmaceutical and biopharmaceutical projects in Switzerland. Opportunities exist for both leadership and hands-on roles.

Senior Bioprocess Engineer specializing in Downstream Processing (DSP) for biopharmaceutical manufacturing. Provide technical leadership, hands-on support, and drive operational excellence in GMP purification operations.