Quality Intern

Spain, Barcelona, Sant Cugat del Vallès

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Main tasks and duties:

  • Assist in the creation and maintenance of the site specific QMS documentation.
  • Assist the Quality Managers team in the review of product deliverables related to medical device software products developed in the R&D department in Sant Cugat or other Roche locations in the established milestones along the product life cycle.
  • Assist in the creation and maintenance of KPIs of the department.
  • Review coherence of documentation (Product Requirements, Product Issues, Product risks) in tools such as HP-ALM.
  • Assist in the creation and review of DQLA SharePoint content.

Additional tasks, duties and responsibilities:

  • To permanently optimize processes to increase quality and efficiency standards.

Requirements:
  • Preferred Education: Recent graduates from University degree or Master in scientific or technological discipline, ideally in Biomedicine, Biotechnology field.
  • No previous experience needed.
  • Fluent command of English.
  • Interest for medical devices, quality management systems and software development processes. Knowledge of quality and regulatory standards is a plus but not mandatory: ISO 13485, FDA QSR. 
  • This position is only available for candidates who have never worked in a company in Spain or used a "contrato de prácticas" before.