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.

109 - Validation Specialist