CQV Specialist 100%.

  • Visp, Valais
  • publié il y a 1 jour
  • se termine 17 avril 2025
postuler

détails du poste

sommaire.

  • catégorie
    administration
  • contact
    Vanuwy Kulasegaram
  • référence
    142523-1711

accélère la candidature en partageant ton profil

détails du poste

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

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

  • qualifications

    • 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

informations de contact.

nous sommes à ta disposition pour toute question.

VK

Vanuwy Kulasegaram

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