QA Technician who provides day-to-day Quality support for the manufacturing lines to ensure continued effective and compliant processes. Key responsibilities include production audits,control of non-conforming product, quality metrics reporting, practice versus, procedure reviews, compliance to GMP and GDP, and supporting process improvements.Responsibilities:Provide quality assurance support for daily operational activities, with a focus on production auditing, non-conforming material management, incoming and in-process inspections, quality metrics reporting, procedure compliance, problem-solving, rework coordination, and process improvement initiatives.Prepare and maintain documentation to support operational effectiveness, product realization, and the Quality Management System (QMS).Deliver day-to-day quality support for manufacturing operations to ensure processes remain effective and compliant.Participate in regular production and planning meetings to provide quality input and oversight.Key Skills:Minimum 2-5 years' experience in an operations role within theMedical Device or Pharmaceutical IndustryExperience and understanding of regulations related to medical devices e.g. ISO 13485, MDR and applicable FDA Requirements.Experience in writing documentation in a regulated environment.Experience in conducting audits in a regulated environment