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. You’ll help ensure materials meet EU and international pharmaceutical standards and contribute to regulatory excellence across the business.
meaningful projects with real impact
global industry leader
Prepare, review and issue technical and regulatory documentation for pharma customers (Quality & Technical Agreements, Supply Chain Statements, Regulatory Questionnaires, Compliance Statements)
Source and evaluate regulatory, quality and technical information from internal and supplier sources
Lead regulatory deliverables for customer-specific projects and coordinate data collection for new product introductions




Support change control evaluations and customer notifications
Work with QHSE and supply chain to ensure compliance with standards (IPEC GMP/GDP, EXCiPACT, GDP, etc)
Contribute to integral Pharma Regulatory projects and harmonisation efforts
Deliver training on regulatory topics to commercial, supply chain and internal teams
Perform other tasks to support regulatory and compliance success
Cross-functional collaboration with commercial and value-added services teams
Fluent in English and Spanish (written and spoken)
Ability to interpret regulations and resolve compliance issues
documentation and compliance drafting
Regulatory Affairs Specialist - Brenntag • granollers, catalunya, es
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📌 Compliance Officer - Spanish (Lérida)
🏢 Brenntag
📍 Lérida