CQA Head

Job Description : CQA Head (Sterile Pharma Manufacturing) UK Open to International candidates Experience: 25+ Years Mandatory: European Regulatory Exposure Minimum 8+ Years of Experience as CQA Head Only candidates from Sterile Pharma Manufacturing Background with European countries exposure will be considered. Key Responsibilities: • Lead and manage overall Corporate Quality Assurance activities for sterile pharmaceutical manufacturing operations. • Ensure compliance with EU-GMP, cGMP, WHO, MHRA, and other international regulatory requirements. • Develop, implement, and maintain Quality Management Systems (QMS). • Review and approve investigations, CAPA, change controls, deviations, and risk assessments. • Lead regulatory inspections and customer audits while ensuring audit readiness across manufacturing facilities. • Drive continuous quality improvement initiatives and maintain a strong quality culture. • Oversee validation, qualification, annual product reviews, and product quality reviews. • Provide strategic direction for compliance, documentation, and data integrity practices. • Collaborate with Production, QC, Engineering, and Regulatory Affairs teams to ensure smooth operations and regulatory compliance. • Mentor and develop quality teams to achieve organizational excellence.

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