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
For our client, a global leader in the life sciences industry based in Visp, we are looking for a Piping Category Specialist and Buyer. The Piping Global Category Expert is a pivotal role responsible for managing procurement category activities for major investment projects. This role coordinates with Capex Lead Buyers and Piping Subject Matter Experts (SMEs) to plan and execute high-complexity projects, primarily at the Visp site, ensuring technical
For our client, a global leader in the life sciences industry based in Visp, we are looking for a Piping Category Specialist and Buyer. The Piping Global Category Expert is a pivotal role responsible for managing procurement category activities for major investment projects. This role coordinates with Capex Lead Buyers and Piping Subject Matter Experts (SMEs) to plan and execute high-complexity projects, primarily at the Visp site, ensuring technical
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
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:
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
Location: Switzerland (100% on-site)Contract type: Full-timeLanguage: German (mandatory); English a strong plusThe roleJoin a growing pharmaceutical site as a CQV Engineer owning validation activities for equipment, systems and facilities. You’ll coordinate installations, author and execute IQ/OQ/PQ protocols, and deliver audit-ready documentation in line with cGMP/GxP and internal procedures.What you’ll doPlan and coordinate CQV for facilities &
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,
Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a
Are you the person who actually enjoys the adrenaline of a surprise inspection? Do you find the "missing link" in a paper trail before anyone else even realizes it’s gone?Our client, a Randstad client, is looking for a Senior QMS & Compliance Expert to join their team in Visp. We need someone who treats Auditing as an art form, Compliance as a religion, and the Quality Management System (QMS) as their personal masterpiece.If you can stare down a
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive
Title: Quality SpecialistLocation: Visp, Valais, Switzerland (On-site)We are looking for a Quality Specialist with experience in deviation investigations and CAPA management within a GMP-regulated environment – ideally with strong knowledge of processes related to monoclonal antibodies.This role is critical to ensuring regulatory compliance, preventing recurring issues, and strengthening the quality system through effective corrective and preventive
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