Quality Specialist (Documentation)

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.

• 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

• 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.