Senior Technical Consultant – Structured Content Authoring

Senior Technical Consultant voor een strategisch transformatieprogramma in de farmaceutische sector, hybride Brussels, fulltime.

Locatie
Brussel, BE
Werkvorm
hybride

Geen duidelijke warme-stoelaanwijzingen in de beschikbare beoordeling.

Bekijk bij Pauwels Consulting (opent in een nieuw tabblad)

Mail mij vergelijkbare opdrachtenZonder CV of account

Je zoekfilterstechnical consultant structured content authoring · Zzp

Elke ochtend een e-mail als er nieuwe opdrachten zijn die passen bij je zoekfilters.

Eisen

  • High attention to detail and a quality-driven mindset
  • Proven track record of translating technical requirements into actionable solution designs
  • Deep understanding of regulatory processes such as Regulatory Affairs, CMC, or Clinical
  • Extensive expertise working within GxP and regulated pharmaceutical environments
  • 8+ years of experience in system integration and technical project coordination
  • Fluent in English
  • Proactive and solution-oriented
  • Experienced in coordinating multiple vendors and cross-functional technical stakeholders

Wensen

  • Experience with Structured Content Authoring platforms or Veeva Vault
  • Knowledge of French
  • Integration experience involving Snowflake, Single Sign-On (SSO), or AI/Agentic capabilities
  • Familiarity with IQVIA, Docuvera, or Ulysses regulatory technology
Volledige omschrijving

Pauwels Consulting is seeking, on behalf of a leading organization in the pharmaceutical sector, a technical consultant to join a strategic transformation program. This role supports the implementation and integration of an intelligent document generation platform to modernize regulatory submissions through structured content and AI-assisted authoring.

Responsibilities: Lead technical discussions with vendors and internal teams to refine integration specifications; Coordinate solution design and implementation activities across enterprise architects and validation experts; Manage technical integrations with data foundations, content management systems, and identity providers; Translate complex business requirements into detailed technical specifications and solution designs; Oversee testing preparation and validation activities to ensure compliance with quality standards; Facilitate stakeholder workshops to drive technical decisions and maintain project momentum.

Requirements: 8+ years of experience in system integration and technical project coordination; extensive expertise working within GxP and regulated pharmaceutical environments; deep understanding of regulatory processes such as Regulatory Affairs, CMC, or Clinical; proven track record of translating technical requirements into actionable solution designs; experienced in coordinating multiple vendors and cross-functional technical stakeholders; high attention to detail and a quality-driven mindset; proactive and solution-oriented; fluent in English.

Nice to haves: Experience with Structured Content Authoring platforms or Veeva Vault; familiarity with IQVIA, Docuvera, or Ulysses regulatory technology; integration experience involving Snowflake, Single Sign-On (SSO), or AI/Agentic capabilities; knowledge of French.

Offer: Start date ASAP; Duration December 2026 + extensions; Work regime Full-time; Location Brussels; Working model Hybrid (minimum 2 days onsite); Contract open to both permanent employees and freelancers.

Bekijk bij Pauwels Consulting (opent in een nieuw tabblad)

Reageren

Senior Technical Consultant – Structured Content Authoring

Je CV en reacties