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Technical Consultant IDGP (Intelligent Document Generation Platform)

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Job Location:

Brussels - Belgium

Monthly Salary: Not provided by the employer
Experience Required: 8years
Posted: 24 October 2026 (2 days ago)
Application Deadline: 21 January 2027
Vacancies: 1 Vacancy

Job Summary

The consultant will join the IDGP (Intelligent Document Generation Platform) initiative within the Ruby Program a strategic transformation program aimed at accelerating regulatory submissions and time-to-market. The project focuses on implementing a structured content authoring platform that will replace traditional document authoring methods and enable content reuse AI-assisted authoring and direct integration of enterprise data into regulatory documents. The role will support the technical implementation and integration of the selected solution with multiple systems and teams.

Typical Day

  • Lead discussions with vendors and internal technical teams.
  • Gather and refine technical requirements and integration specifications.
  • Coordinate solution design and implementation activities.
  • Work closely with Enterprise Architects DT teams validation SMEs and business stakeholders.
  • Follow up on integrations with SSO Snowflake/Data Foundation Veeva and AI/Agentic capabilities.
  • Support testing preparation validation activities and implementation readiness.
  • Facilitate workshops and stakeholder meetings to drive technical decisions and project progress.


Benefits

Years of Experience

  • Target profile: 5-8 years of relevant experience.
  • Manager preference is towards the higher end of the range due to the complexity of the integrations and stakeholder environment.

Must Have

  • Strong experience in system integration projects.
  • Experience working in a GxP / regulated pharmaceutical environment.
  • Understanding of regulatory processes (Regulatory Affairs CMC Labeling Clinical etc.).
  • Experience translating technical requirements into specifications and solution designs.
  • Ability to coordinate multiple stakeholders and vendors.
  • Strong communication skills and autonomy.
  • High attention to detail and quality mindset



Required Skills:

8 Years experience in system integration projects Experience working in a GxP / regulated pharmaceutical environment Understanding of regulatory processes Ability to coordinate multiple stakeholders and vendors At least 4 years experience with digital transformation project related to content authoring platform Experience implementing and integrating AI-assisted authoring


Required Education:

University degree or similar