Job description
Turn complex regulatory challenges into elegant digital solutions.
Join a flagship program that is redefining how life-science organizations create, manage, and submit regulatory content worldwide. As our IDGP Business Analyst you will own the requirements lifecycle for next-generation structured-authoring platforms and help bring critical therapies to patients faster.
Your mission in one line
Transform multi-disciplinary needs into crystal-clear requirements that power structured-content solutions across Labelling, CMC, Clinical, and Non-clinical domains.
A day that makes an impact
* Run discovery sessions with regulatory experts to surface functional & non-functional needs
• Distill findings into concise user stories, acceptance criteria, and traceability matrices
• Drive RFI/RFP cycles: craft documentation, score vendor proposals, and orchestrate demos & POCs
• Partner with Process, Data, IT, and AI squads to embed AI use-cases into the roadmap
• Facilitate workshops, manage stakeholder expectations, and deliver transparent progress reports
What you bring
Must-have
• 3–8 years as a Business Analyst in cross-functional or highly regulated environments
• Proven ability to capture, structure, and document complex requirements end-to-end
• Hands-on experience supporting RFI/RFP processes and vendor evaluations
• Solid project-management toolkit: scope, timeline, risk, and stakeholder management
• Comfort working at the intersection of business and technology
• Advanced English (C1–C2) – you will present to global audiences
Nice-to-have
• Background in pharma, medical devices, or other life-science sectors
• Familiarity with CTD submission dossiers and regulatory workflows
• Exposure to Structured Content Authoring or Veeva Vault RIM
• Experience defining AI/ML use-cases or data-driven process improvements
• French language skills (a bonus, not a barrier)
Why joining us?
* Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees.
* Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions.
* International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe.