25 sep
|
Brenntag
|
Lérida
Brenntag is seeking a Regulatory Affairs Specialist to support regulatory, quality and product stewardship for a pharma raw materials portfolio in the Barcelona/Valencia area.
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You will deliver audit-ready documentation and drive regulatory deliverables for bespoke projects, collaborating across functions and occasionally traveling to supplier meetings and audits.
Responsibilities include xqbhyrx preparing regulatory documents, ensuring alignment with GMP/GDP and pharmacopoeia, sourcing regulatory
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📌 Pharma Regulatory Affairs Specialist – Global Compliance (Lérida)
🏢 Brenntag
📍 Lérida