Corporate QA – (CSV) Specialist

We’re supporting a well-established biologics pharmaceutical organisation 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 1–2 days per week) with flexible remote working, and sit within highly regulated GMP environments across both manufacturing and corporate quality functions.

This role sits at the intersection of Quality Assurance, IT systems, and regulatory compliance, ensuring computerised systems remain validated, compliant, and fit for purpose throughout their lifecycle.

Typical systems include LIMS, QMS, MES, ERP (such as SAP), and electronic document management platforms.

Key responsibilities:

• Ensuring validation and compliance of computerized systems in GMP environments
• Supporting lifecycle management of regulated digital sy...