Technical Consultant - IDGP (Intelligent Document Generation Platform)

NextLink Group; Anderlecht; On-site; EUR 70,000 - 110,000; Full time

Job summary

NextLink Group is seeking a Technical Consultant for the IDGP initiative in Bruxelles Anderlecht, Belgium. You will join a strategic program to implement a structured content authoring platform and integrate it with multiple systems, enabling data reuse, AI-assisted authoring, and enterprise data integration for regulatory documents.

The role requires 5–8+ years of relevant experience in system integration within a GxP/regulatory environment, with strong stakeholder coordination and technical

Qualifications

• Experience in system integration projects, preferably in regulated environments.
• Knowledge of GxP and regulatory processes (Regulatory Affairs, CMC, Labeling, Clinical).
• Ability to translate technical requirements into specs and designs.
• Proven coordination of multiple stakeholders and vendors.
• Strong communication skills and autonomy.
• High attention to detail and quality mindset.

Responsibilities

• 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.

Skills

System integration

GxP regulation

Regulatory processes

Requirements analysis

Stakeholder coordination

Communication

Attention to detail

Job description

Technical Consultant - IDGP (Intelligent Document Generation Platform)

Bruxelles Anderlecht, Belgium | Posted on 10/23/2026

What is the mission about?

see JD

Job Description

The consultant will join the IDGP (Intelligent DocumentGeneration Platform) initiative within the Ruby Program, a strategictransformation program aimed at accelerating regulatory submissions andtime-to-market. The project focuses on implementing a structured contentauthoring platform that will replace traditional document authoring methods andenable content reuse, AI-assisted authoring, and direct integration ofenterprise data into regulatory documents. The role will support the technicalimplementation and integration of the selected solution with multiple systemsand teams.

Typical Day

• Leaddiscussions with vendors and internal technical teams.
• Gatherand refine technical requirements and integration specifications.
• Coordinatesolution design and implementation activities.
• Workclosely with Enterprise Architects, DT teams, validation SMEs, andbusiness stakeholders.
• Followup on integrations with SSO, Snowflake/Data Foundation, Veeva andAI/Agentic capabilities.
• Supporttesting preparation, validation activities, and implementation readiness.
• Facilitateworkshops and stakeholder meetings to drive technical decisions andproject progress.

Years of Experience

• Targetprofile: 5-8+ years of relevant experience.
• Managerpreference is towards the higher end of the range due to the complexity ofthe integrations and stakeholder environment.

Must Have

• Strongexperience in system integration projects.
• Experienceworking in a GxP / regulated pharmaceutical environment.
• Understandingof regulatory processes (Regulatory Affairs, CMC, Labeling, Clinical,etc.).
• Experiencetranslating technical requirements into specifications and solutiondesigns.
• Abilityto coordinate multiple stakeholders and vendors.
• Strongcommunication skills and autonomy.
• High attention to detail and quality mindset