Descripción de la oferta
We’re supporting a well‑established biologics pharmaceutical organization based in Catalonia, Spain, currently undergoing a significant expansion across its manufacturing and quality operations.
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 global markets.
Key responsibilities:
Managing and maintaining GMP‑controlled documentation and records
Supporting product registrations across multiple countries
Maintaining specifications, analytical methods, SOPs, and change controls
Ensuring compliance with GMP and pharmacopoeia requirements
Working closely with Quality Control and Regulatory Affairs teams
What we’re looking for:
Strong understanding of GMP environments
Experience with controlled quality documentation systems
Familiarity with analytical methods and regulatory documentation
Strong Microsoft Office and structured documentation skills
Scientific or technical academic background
This role offers the chance to join a growing international organization at a pivotal stage of expansion, with strong development opportunities across quality, validation, and corporate systems.
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