Job Description
0 Teilen For an international pharmaceutical company located in VISP we are looking for a CQV Lead :
JOB DESCRIPTIONProvide leadership of CQV activities in assigned Projects together with PM, Process Engineers and QA Act as subject matter expert (SME) on CQV standards Correct CQV project staffing, expertise and coaching to the CQV staff assigned to projects Initiate necessary training on CQV-Staff / Project staff on CQV and CSV (supported by local CQV -Staff) Keep oversight on CQV -standards, -timelines (etc.) Address immediate time/quality constraints and act adequately Force RFT thinking and approach Consider EHS Requirements Develop and deliver CQV Documents Commissioning Documents (Suppliers / Process Engineers/EMR) QV-Documents (Suppliers / QV-Team /QA) Responsible for ensuring that SGIE projects in Visp are compliant with the global CQV guidelines, aligned ...
JOB DESCRIPTION
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- Location visp, valais
- Job Type Full-time
- Category PLA
- Posted Date June 06, 2026
- Application Deadline July 16, 2026