CQV Specialist 100%
Randstad (Switzerland) Ltd.
Date de publication :
10 janvier 2025Taux d'activité :
100%- Lieu de travail :Visp
job details
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
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qualifications
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Bachelor's Degree in a Science or Technical field
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Proficiency in English, both written and spoken.
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3-6 years of experience in the pharmaceutical industry
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Exceptional technical writing skills with the ability to thoroughly, accurately, and promptly document all work.
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Strong written and verbal communication skills, enabling effective interdepartmental collaboration
- Excellent organizational and time management skills
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