Für die Lonza AG in Visp suchen wir ab sofort einen Scheduler 100% (m/w/d). Key ResponsibilitiesE2E Scheduling: Own and manage end-to-end program schedules for Operational ReadinessWorkload Management: Update and track resource workload for PCP manufacturing buildingsStakeholder Lead: Lead meetings with internal teams (QA, QC, Ops, MSAT, Plant Eng.) for schedule updates and trackingProject Support: Support general planning tasks beyond core scheduling to
Für die Lonza AG in Visp suchen wir ab sofort einen Scheduler 100% (m/w/d). Key ResponsibilitiesE2E Scheduling: Own and manage end-to-end program schedules for Operational ReadinessWorkload Management: Update and track resource workload for PCP manufacturing buildingsStakeholder Lead: Lead meetings with internal teams (QA, QC, Ops, MSAT, Plant Eng.) for schedule updates and trackingProject Support: Support general planning tasks beyond core scheduling to
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
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