Pharma Regulatory Affairs Specialist – EMEA

Airbus; Granollers; Presencial; EUR 42.000 - 56.000; Jornada completa

Descripción de la vacante

Brenntag is seeking a Regulatory Affairs Specialist to join our Pharma team in Barcelona or Valencia. You will support regulatory deliverables across the EU, prepare audit-ready documentation for pharma customers, and coordinate with suppliers to ensure compliant materials.

You will collaborate with commercial, supply chain and QA teams, ensuring documentation accuracy and alignment with EU pharmacopoeia and GDP/GMP standards. Travel for supplier meetings and audits may be required.

Formación

• Degree in life science or equivalent with knowledge of pharmaceutical regulations.
• Experience documenting regulatory and quality information for APIs and excipients.
• Familiarity with EU GDP/GMP, IPEC guidelines and compliance standards.

Responsabilidades

• Prepare, review, and issue regulatory documentation required by pharmaceutical customers.
• Source regulatory information from internal and supplier sources and assess suitability for pharma use.
• Log, track, and report customer documentation requests using defined KPIs.
• Lead regulatory deliverables for customer projects and coordinate data collection for new products.
• Support compliance with IPEC GMP/GDP, EXCiPACT, GDP and other regulatory frameworks.
• Collaborate with commercial, supply chain and QA teams, deliver regulatory training.

Conocimientos

Fluent English

Fluent Spanish

Regulatory expertise

Documentation skills

Cross-functional collaboration

Travel willingness

Educación

Life science degree

Descripción del empleo

Brenntag is seeking a Regulatory Affairs Specialist to join our Pharma team in Barcelona or Valencia. You will support regulatory deliverables across the EU, prepare audit-ready documentation for pharma customers, and coordinate with suppliers to ensure compliant materials.

You will collaborate with commercial, supply chain and QA teams, ensuring documentation accuracy and alignment with EU pharmacopoeia and GDP/GMP standards. Travel for supplier meetings and audits may be required.