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 the
Medical Device or Pharmaceutical Industry
Experience and understanding of regulations related to medical devices e.g. ISO *****, MDR and applicable FDA Requirements.
Experience in writing documentation in a regulated environment.
Experience in conducting audits in a regulated environment