Our client, a leading organization in the pharmaceutical sector, is undergoing a major end-to-end digital transformation within their R&D department to modernize clinical and regulatory processes. The project aims to replace outdated ways of working with a data-driven operating model, requiring the translation of high-level designs into actionable, compliant workflows. This role serves as a crucial implementation bridge between target-state design and sustainable global execution. Translate future-state process designs into detailed, implementable workflows and operating practices. Facilitate workshops with process owners and subject matter experts to capture and structure process details. Refine governance models and define responsibilities to harmonize global operating practices. Develop standardized procedural documentation including SOPs, guidelines, templates, and KPIs. Bridge the gap between design and execution to ensure process adoption and long-term sustainability. Identify process gaps and improvement opportunities within an agile, product-oriented squad environment. What are we looking for? 5+ years of experience in process engineering and complex process analysis. Experience working within large-scale digital transformation programs or agile, product-oriented environments. 3+ years of experience in workflow re-engineering and technical process documentation. You possess structured thinking skills with knowledge of Six Sigma or Black Belt methodologies. You have the ability to navigate and operate effectively within ambiguous, matrixed organizational structures. You bring strong stakeholder collaboration and project coordination skills. You possess a proactive, solution-oriented mindset with the ability to work autonomously. You are fluent in English. Nice to Haves Previous experience in pharmaceutical, biotech, or R&D environments. Knowledge of GxP and Data Integrity principles. Exposure to human-centric process design or transformation methodologies. Experience within specific R&D domains such as CMC, regulatory, or clinical development. What do we offer? Start date: ASAP Duration: until November Work regime: Full-time % considered) Location: Belgium Working model: Hybrid or Remote with occasional onsite travel for major meetings Contract: open to both permanent employees and freelancers