Für die Lonza AG in Visp suchen wir ab sofort eine/n Bioprocess Engineer 100% (w/m/d) Deine KernaufgabenKampagnenleitung: Du verantwortest die Herstellung von Biokonjugaten unter cGMP-RichtlinienProzess-Support: Du sicherst die Chargenausführung, löst technische Probleme an den Anlagen und wertest Testergebnisse ausCompliance: Du übernimmst die lückenlose GMP-Dokumentation sowie das Erstellen von Kampagnenberichten und RisikoanalysenOptimierung:
Für die Lonza AG in Visp suchen wir ab sofort eine/n Bioprocess Engineer 100% (w/m/d) Deine KernaufgabenKampagnenleitung: Du verantwortest die Herstellung von Biokonjugaten unter cGMP-RichtlinienProzess-Support: Du sicherst die Chargenausführung, löst technische Probleme an den Anlagen und wertest Testergebnisse ausCompliance: Du übernimmst die lückenlose GMP-Dokumentation sowie das Erstellen von Kampagnenberichten und RisikoanalysenOptimierung:
For our client, a global leader in the life sciences industry based in Visp, we are looking for a highly experienced CQV Engineer. The CQV Engineer is a critical role responsible for the commissioning, qualification, and validation of equipment and facilities. This role ensures that all installations meet stringent regulatory and technical standards, coordinating across departments to move projects from installation to full GMP compliance. General
For our client, a global leader in the life sciences industry based in Visp, we are looking for a highly experienced CQV Engineer. The CQV Engineer is a critical role responsible for the commissioning, qualification, and validation of equipment and facilities. This role ensures that all installations meet stringent regulatory and technical standards, coordinating across departments to move projects from installation to full GMP compliance. General
Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and
Role OverviewWe are looking for an experienced Commissioning, Qualification & Validation (CQV) Engineer to support validation activities within a highly regulated pharmaceutical manufacturing environment.In this role, you will contribute to the commissioning, qualification, and validation of equipment, systems, and facilities, ensuring compliance with cGMP requirements and industry regulations.You will collaborate closely with engineering, quality, and
Senior SAP Basis Engineer (Remote)We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting complex SAP landscapes. In this role, you will be responsible for the administration, optimization, and reliability of SAP systems, ensuring high performance, security, and alignment with business objectives.This is a fully remote position, ideal for someone who thrives in an autonomous work environment while
Senior SAP Basis Engineer (Remote)We are seeking an experienced and proactive Senior SAP Basis Engineer to join a global IT team supporting complex SAP landscapes. In this role, you will be responsible for the administration, optimization, and reliability of SAP systems, ensuring high performance, security, and alignment with business objectives.This is a fully remote position, ideal for someone who thrives in an autonomous work environment while
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
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