At Visium, we enable enterprise executives in defining their AI & Data strategy, execute large scale transformations and implement AI across operations, ensuring their organization becomes future-proof. With expertise in strategy, architecture, cloud engineering, analytics, artificial intelligence and machine learning, we empower our clients to unleash and scale the power of their data. We're on a mission to pioneer a bright future and build future‑proof and ethical organizations. Join the curious, the ambitious, the doers, the good‑hearted, the ones who build a world we're all in awe of – our Visumees.RoleAs Business Development Director for Regulatory Affairs, you will lead commercial activities for Visium's Scribe offering, an AI agent platform purpose‑built for regulatory document drafting in Life Sciences. You will be the primary point of contact for pharmaceutical and biotech organisations looking to accelerate their regulatory submissions, reduce authoring time, and maintain full compliance with FDA, EMA, and GxP requirements. At Visium, you will play a pivotal role in driving the growth of Scribe, helping enterprise clients transform how their regulatory and quality teams produce CTD modules, CSRs, APQRs, and GVDs. This is a high‑impact, entrepreneurial position where your deep understanding of the regulatory affairs landscape, combined with strong relationship‑building and strategic sales skills, will directly shape how leading Life Sciences organisations adopt AI‑driven document workflows.ResponsibilitiesClient Acquisition & Revenue GrowthLead the identification, engagement, and acquisition of new enterprise clients in pharmaceuticals, biotechnology, medtech, and regulatory affairs functions within healthcare organisationsDevelop and execute strategic outbound initiatives,



including executive‑level networking within regulatory and quality affairs communities, thought leadership engagements, and targeted outreach to heads of Regulatory Affairs, CMC, and Clinical OperationsQualify and prioritise opportunities to align Visium's Scribe platform with client submission timelines, document automation needs, and compliance objectivesSolution Discovery & Client AlignmentConduct discovery meetings with VP/Head‑level Regulatory Affairs, Quality, and R&D stakeholders to understand submission bottlenecks, authoring inefficiencies, and compliance requirements across FDA, EMA, and GxP frameworksShape tailored proposals and presentations that demonstrate how Scribe accelerates regulatory document production — from CTD modules and CSRs to APQRs and GVDs — while keeping human experts in full control of every submissionCollaborate with Visium's delivery and product teams to ensure successful onboarding, configuration to client templates and data systems, and measurable impact on authoring time and submission lead timesMaintain deep knowledge of the regulatory affairs landscape, including evolving FDA and EMA guidance, industry trends in AI‑assisted document workflows, and the competitive environment for regulatory technology solutionsLeadership & Team DevelopmentMentor and develop junior business development and client engagement professionals,



building commercial acumen and domain expertise in regulatory affairs and Life SciencesDrive a culture of collaboration across sales, delivery, and marketing teams to maximise client impact and grow Scribe's presence in the marketDefine performance goals, track pipeline progress, and share market insights to continuously optimise team effectiveness and go‑to‑market strategyRequirements6-8 years of experience in business development, client engagement, or strategic consulting within the Life Sciences sector, with direct exposure to regulatory affairs, quality, or clinical functionsProven ability to drive enterprise client acquisition and revenue growth in complex, regulated industries, ideally with experience selling software, AI, or technology solutions into regulatory or quality teamsStrong understanding of regulatory submission processes, document types (CTD, CSR, APQR, GVD), and compliance frameworks (FDA, EMA, GxP)Excellent communication, presentation, and relationship‑building skills with VP and C‑level stakeholders in regulated environmentsEntrepreneurial mindset, strategic thinker, and highly results‑oriented, comfortable operating in a fast‑growing, product‑led companyFluent in English; German or French is considered a strong plus given Visium's European client baseBenefitsA competitive compensation packageA yearly education budget to steep your learning curveA yearly sport budget because a fit body leads to a fit mindA adaptable working culture because your work‑life balance matters to usA position that enables you to have an impact on 1'000s of people, and the whole company's growthAn international, knowledgeable, and passionate team with a strong collaborative mindset#J-18808-Ljbffr

📌 Business Development Director (Life Science & R&D) (Mislata)
🏢 GFT
📍 Mislata