Overview
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.
Compensaciones / Beneficiosinternational, collaborative environmentcontinuous learning and career developmentmeaningful projects with real impactequal employment opportunitiesglobal industry leader
ResponsabilidadesPrepare, 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 teams
Requisitos principalesDegree in life science or equivalent experienceStrong knowledge of APIs, excipients, biopharma materials, and traditional