CQV Specialist 100%

For Lonza in Visp Randstad (Switzerland) AG is looking for a CQV Specialist for 8 months (July 2025)

Job description:

• Oversee facilities, utilities, validation lifecycle, technical documentation, and processes, including GAP analysis and risk assessment
• Develop and manage validation documentation (URS, DQ, FMEA, FAT, SAT, IQ, IOQ, OQ, PQ)
• Execute validation protocols (IQ/OQ/PQ) for equipment, systems, and utilities
• Prepare detailed reports on validation activities and identify process efficiencies
• Stay updated on industry regulatory changes and incorporate lessons learned
• Perform Quality Systems tasks (Document Management, Change Control, Non-Conformities, CAPAs)
• Draft and revise engineering-related procedures
• Support engineering in validation, requalification, and maintenance efforts
• Handle additional duties as assigned

• Bachelor's Degree in a Science or Technical field

• Proficiency in English, both written and spoken.

• 3-6 years of experience in the pharmaceutical industry

• Exceptional technical writing skills with the ability to thoroughly, accurately, and promptly document all work.

• Strong written and verbal communication skills, enabling effective interdepartmental collaboration

• Excellent organizational and time management skills