Join Brenntag as a Regulatory Affairs Specialist in the Barcelona/Valencia area to support regulatory, quality, and product stewardship for a broad pharma raw materials portfolio. You will deliver accurate, audit-ready documentation to pharmaceutical customers and drive regulatory deliverables for bespoke projects. The role involves cross-functional collaboration, process improvement, and occasional travel to supplier meetings and audits. You’ll help ensure materials meet EU and international pharmaceutical standards and contribute to regulatory excellence across the business.continuous learning and career developmentmeaningful projects with real impactequal employment opportunitiesglobal industry leaderPrepare, review and issue technical and regulatory documentation for pharma customers (Quality & Technical Agreements, Supply Chain Statements, Regulatory Questionnaires, Compliance Statements)Ensure documents align with pharmacopoeia, IPEC Guidelines, EU GDP and GMPSource and evaluate regulatory, quality and technical information from internal and supplier sourcesLog,



track and report customer documentation requests using KPIs and identify process improvementsLead regulatory deliverables for customer-specific projects and coordinate data collection for new product introductionsSupport change control evaluations and customer notificationsWork with QHSE and supply chain to ensure compliance with standards (IPEC GMP/GDP, EXCiPACT, GDP, etc)Contribute to general Pharma Regulatory projects and harmonisation effortsDeliver training on regulatory topics to commercial, supply chain and internal teamsPerform other tasks to support regulatory and compliance successCross-functional collaboration with commercial and value-added services teamsDegree in life science or equivalent experienceStrong knowledge of APIs, excipients, biopharma materials, and traditional pharma materialsUnderstanding of European National Competent Authority requirements for distribution of APIs and raw materialsFluent in English and Spanish (written and spoken)Strong written communication to produce compliant documentationExcellent collaboration and proactive cross-functional workAbility to interpret regulations and resolve compliance issuesHigh attention to detail and organisational skillsWillingness to travel occasionallyproactive mindsetpharmaceutical regulatory knowledge (APIs, excipients)GMP/GDP, IPEC, EXCiPACTdocumentation and compliance draftingRegulatory Affairs Specialist - Brenntag • granollers, catalunya, es

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📌 Regulatory Affairs Specialist - Brenntag (Madrid)
🏢 Brenntag
📍 Madrid