GMP Materials Inspector & Release Analyst

A leading biopharmaceutical company in Greater London seeks a Quality Control Specialist to manage incoming materials and support GMP-compliant activities. Responsibilities include performing inspections of raw materials, maintaining documentation to GMP standards, and ensuring material status for release. Ideal candidates should have at least 1 year of experience in a GxP environment and proficiency in Microsoft Office. This role offers the opportunity to contribute significantly to quality assurance in an innovative sector.