Cqv specialist 100%

Vor 2 Tagen


Visp, Schweiz Randstad Vollzeit
Jobdescription 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 Qualifikationen 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
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