IDGP Technical Consultant - Regulatory Document Platform

Next-Link; Anderlecht; Sur place; EUR 70 000 - 110 000; Plein temps

Résumé du poste

Next-Link in Bruxelles Anderlecht, Belgium is seeking a Technical Consultant for the IDGP initiative within the Ruby Program. You will lead integration efforts across vendors and internal teams, translate technical requirements into specs, and coordinate design and implementation with architects and stakeholders.

The role requires 5–8+ years of relevant experience in system integration within a regulated pharmaceutical environment, with strong regulatory process understanding and excellent

Qualifications

• 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.

Responsabilités

• 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.

Connaissances

System integration

GxP experience

Regulatory affairs knowledge

Requirements-to-design translation

Stakeholder coordination

Communication skills

Attention to detail

Description du poste

Next-Link in Bruxelles Anderlecht, Belgium is seeking a Technical Consultant for the IDGP initiative within the Ruby Program. You will lead integration efforts across vendors and internal teams, translate technical requirements into specs, and coordinate design and implementation with architects and stakeholders.

The role requires 5–8+ years of relevant experience in system integration within a regulated pharmaceutical environment, with strong regulatory process understanding and excellent