FAT / CQV Engineer – Pharmaceutical Equipment

Company: Discover International Agency

  • Location: Emilia-Romagna, Italy
  • Seniority: Senior
  • Employment type: Contract
  • Posted: 13 days ago
  • Offer language: English

Job description

FAT / CQV Engineer – Pharmaceutical Equipment | 6-Month Contract | Italy

Discover International is supporting a pharmaceutical manufacturing project in Italy and is looking for an experienced FAT / CQV Engineer to support equipment testing and qualification activities.

This is a hands-on, site-based assignment, with a strong focus on pharmaceutical manufacturing equipment, supplier coordination and technical issue resolution during FAT.

Key responsibilities will include:

  • Witnessing and supporting FAT activities for pharmaceutical production equipment
  • Reviewing FAT protocols, test documentation and technical attachments
  • Verifying equipment functionality against approved specifications and requirements
  • Identifying deficiencies, deviations and punch-list items
  • Supporting technical troubleshooting with equipment suppliers
  • Following corrective actions and modifications through to closure
  • Supporting commissioning and qualification activities where required
  • Maintaining accurate FAT and technical documentation
  • Working closely with engineering, CQV and supplier teams throughout execution

We are particularly interested in candidates with:

  • Approximately 5–10 years of experience within pharmaceutical engineering, CQV, commissioning or equipment qualification
  • Hands-on experience with FAT and/or SAT
  • Strong understanding of pharmaceutical manufacturing machinery and equipment
  • Experience working directly with equipment vendors / OEMs
  • Exposure to aseptic or sterile manufacturing environments
  • Practical experience managing equipment deficiencies, troubleshooting and punch lists
  • Ability to work independently in a hands-on individual contributor capacity
  • Good knowledge of GMP requirements

Contract details:

  • Duration: 6 months
  • Location: Italy
  • Working model: Full-time onsite, 5 days per week
  • Contract: B2B / consulting
  • Start: As soon as possible

Italian language capability would be highly advantageous.

Ingegnere FAT / CQV – Apparecchiature Farmaceutiche | Contratto di 6 mesi | Italia

Discover International sta supportando un progetto nel settore della produzione farmaceutica in Italia ed è alla ricerca di un/una FAT / CQV Engineer con esperienza nelle attività di testing, commissioning e qualifica di apparecchiature farmaceutiche.

Si tratta di un incarico operativo e onsite, con particolare attenzione alle apparecchiature di produzione farmaceutica, al coordinamento con i fornitori e alla gestione tecnica delle problematiche emerse durante le attività di FAT.

Principali responsabilità:

  • Partecipare e fornire supporto durante le attività di FAT su apparecchiature di produzione farmaceutica
  • Revisionare protocolli FAT, documentazione di test e allegati tecnici
  • Verificare la funzionalità delle apparecchiature rispetto alle specifiche e ai requisiti approvati
  • Identificare anomalie, deviazioni, deficiency e punch-list item
  • Supportare il troubleshooting tecnico insieme ai fornitori delle apparecchiature
  • Monitorare azioni correttive e modifiche tecniche fino alla completa chiusura
  • Supportare, ove necessario, attività di commissioning e qualification
  • Garantire la corretta gestione e completezza della documentazione FAT e tecnica
  • Collaborare con i team Engineering, CQV e con i fornitori durante l'esecuzione delle attività

Profilo ricercato:

  • Circa 5–10 anni di esperienza in ambito pharmaceutical engineering, CQV, commissioning o equipment qualification
  • Esperienza pratica in attività di FAT e/o SAT
  • Buona conoscenza di macchinari e apparecchiature per la produzione farmaceutica
  • Esperienza nel rapporto diretto con fornitori di apparecchiature / OEM
  • Esperienza in ambienti di produzione sterile o asettica
  • Esperienza pratica nella gestione di problematiche tecniche, troubleshooting, deficiency e punch list
  • Capacità di lavorare in autonomia in un ruolo operativo e hands-on
  • Buona conoscenza dei requisiti GMP

Dettagli contrattuali:

  • Durata: 6 mesi
  • Sede: Italia
  • Modalità di lavoro: Full-time onsite, 5 giorni a settimana
  • Contratto: B2B / consulenza
  • Inizio: Il prima possibile

La conoscenza della lingua italiana rappresenta un importante vantaggio.

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