Quality Systems Pharmacist
Aspen
Posted 21 October 2026
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Start free — we apply for you →To support the Quality System by ensuring accurate product and manufacturing data, compliant documentation and effective quality processes in line with GMP and regulatory requirements. Quality System Support Provide support for Quality and IT systems. Oversight and verification of manufacturing processes to verify compliance with GMP and regulatory requirements. Support quality reviews, investigations and corrective actions. Master Data & MBR Management Maintain critical product and master data. Create and maintain Master Batch Records (MBRs). Ensure MBRs are accurate, complete and GMP compliant. Manage MBR changes and validations. Document Management Develop, review and maintain SOPs and quality documents. Ensure appropriate document control and version management. Maintain quality records and ensure data integrity. Audits & Compliance Support internal, external and regulatory audits. Conduct root cause analysis and risk assessments. Support ongoing GMP compliance and quality system reviews. Planning & Support Provide technical and operational quality support. Monitor relevant legislation, regulations and industry developments. Provide quality information and reports as required.