Descripción de la oferta
We’re supporting a well-established biologics pharmaceutical organisation based in Catalonia, Spain, currently undergoing a significant expansion across its manufacturing and quality operations.Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura.This position offers a strong mix of on‑site collaboration (typically 3‑4 days per week) with flexible remote working, and sit within highly regulated GMP environments across both manufacturing and corporate quality functions.This role focuses on ensuring the integrity, control, and lifecycle management of regulated pharmaceutical documentation across general markets.Key responsibilitiesManaging and maintaining GMP‑controlled documentation and recordsSupporting product registrations across multiple countriesMaintaining specifications, analytical methods, SOPs, and change controlsEnsuring compliance with GMP and pharmacopoeia requirementsWorking closely with Quality Control and Regulatory Affairs teamsWhat we’re looking forStrong understanding of GMP environmentsExperience with controlled quality documentation systemsFamiliarity with analytical methods and regulatory documentationStrong Microsoft Office and structured documentation skillsScientific or technical academic backgroundThis role offers the chance to join a growing international organisation at a pivotal stage of expansion, with strong development opportunities across quality, validation, and corporate systems.
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