ppWe’re supporting a well‑established biologics pharmaceutical organization based in Catalonia, Spain, currently undergoing a significant expansion across its manufacturing and quality operations. /p pThis position offers a strong mix of on‑site collaboration (typically 3‑4 days per week) with adaptable remote working, and sit within highly regulated GMP environments across both manufacturing and corporate quality functions. /p pThis role focuses on ensuring the integrity, control, and lifecycle management of regulated pharmaceutical documentation across global markets. /p h3Key responsibilities: /h3 ul liManaging and maintaining GMP‑controlled documentation and records /li liSupporting product registrations across multiple countries /li liMaintaining specifications, analytical methods, SOPs,
and change controls /li liEnsuring compliance with GMP and pharmacopoeia requirements /li liWorking closely with Quality Control and Regulatory Affairs teams /li /ul h3What we’re looking for: /h3 ul liStrong understanding of GMP environments /li liExperience with controlled quality documentation systems /li liFamiliarity with analytical methods and regulatory documentation /li liStrong Microsoft Office and structured documentation skills /li liScientific or technical academic background /li /ul pThis 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. /p /p #J-18808-Ljbffr