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 integral 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.

📌 Quality Specialist (Documentation) (Madrid)
🏢 Hlx Life Sciences
📍 Madrid