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
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Je zoekfilterstechnical consultant structured content authoring · Zzp
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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.
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