Cure Talent is thrilled to partner with a leading Pharmaceutical CDMO who, due to their exceptional continued growth, have an exciting opportunity for a Senior Quality Associate to join their team. In this role, you will take a lead in maintaining and developing the Pharmaceutical Quality System across UK and Ireland operations. You will provide specialist QA support across the full range of Quality Systems, including deviations, CAPA, change control, validation, supplier audits, and document control. You’ll also play a key role in hosting audits, training QA Officers, and supporting cross-functional teams to ensure operational compliance with GMP and GDP regulations. Key Responsibilities: * Maintain and develop the company’s global PQS in line with current regulations and internal standards * Oversee core PQS elements including change controls, CAPAs, deviations, complaints, document control, and risk management * Provide QA support for validation, environmental monitoring, and technical documentation * Review and approve batch records, QC test data, and finished product specifications * Support and host internal, supplier, and regulatory audits * Mentor and train QA Officers, delivering internal training on GMP and GDP requirements * Collaborate with production and technical teams to ensure compliance across manufacturing, storage, and distribution * Contribute to management reviews and pre...