Reporting to the Quality Systems Manager, the QA Officer will be responsible for Ensuring the Quality Management System is Robust, Compliant, and Aligned with Regulatory Requirements The QA Officer will Support Quality Oversight, Across Manufacturing, Documentation, Supplier Management, Risk Assessment, and Regulatory Submissions to Maintain the Highest Standards of Product Quality and Regulatory Compliance ROLE Duties Broadly Include Quality Management System Documentation and Controlled Documents Regulatory and Compliance Quality Operations Supplier and Vendor Quality KPIs and Reporting REQUIRED Qualifications and Experience Requirements Include Bachelor s Degree in Pharmaceutical Sciences, Chemistry, Life Sciences, Quality Management, or Closely Related Field Strong Knowledge of cGMP, GDP, ISO Standards, and MHRA/FDA Regulatory Requirements Experience in a Pharmaceutical, Medical Device, or Regulated GMP Environment Hands-On Experience with QMS Operations eg Change Control, Deviations, CAPA s, Document Management Experience Preparing for Internal/External Regulatory Audits. Experience with Batch Documentation, (BPR/Bar Review) and Manufacturing Quality Oversight Experience with ERP Systems eg Sage Excellent Attention to Detail and Accuracy Strong Organisational and Time Management Capabilities Strong Written and Effective Communication Skills Ability to Work Cross Functionally with Multiple Departments Analytical Approach with Strong Problem Solving Skills Ability to ..... full job details .....