Validation Specialist
Trovato in: Talent IT C2 - 3 settimane fa
C&P Engineering, a ProductLife Group Company, is looking for a Validation Specialist.
Fully onsite / hybrid at Florence
Group 10 Responsibilities
The figure will deal with validation activities of control systems and SW applications used for the management of processes in the pharmaceutical and related fields. The figure will be involved in projects aimed at ensuring compliance with reference standards. The candidate will be responsible for drafting qualification/validation protocols, SOPs, and carrying out field testing activities in accordance with predefined standards.
Group 12 Experience
Minimum experience in the sector (minimum 1 year), carried out within consulting companies or pharmaceutical companies in the validation of computerized systems. A good knowledge of the English language (written/oral) is required. Personal flexibility and proactivity complete the profile. The candidate’s ability to work in a team, willingness to travel frequently both in Italy and abroad , and proactivity and flexibility in carrying out the required activities are an integral part of the profile. The selection is aimed at a rapid integration into the work team.
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Validation Specialist
Trovato in: Whatjobs IT C2 - 3 settimane fa
Florence, Italia ProductLife Group A tempo pienoC&P Engineering, a ProductLife Group Company, is looking for a Validation Specialist. Fully onsite / hybrid at Florence Group 10 Responsibilities The figure will deal with validation activities of control systems and SW applications used for the management of processes in the pharmaceutical and related fields. The figure will be...
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CSV Specialist
Trovato in: Whatjobs IT C2 - 1 settimana fa
Florence, Italia Amaris Consulting A tempo pienoJob description CSV SPECIALIST - PHARMA INDUSTRY Cosa farai? Eseguire attività di Validation dei sistemi informatici (CSV) relative ai sistemi di produzione. Garantire il rispetto delle linee guida normative e degli standard dell'industria farmaceutica coerentemente alle normative GMP. Collaborare con...