Job Purpose:The Quality Technician plays a crucial role in ensuring that products adhere to the necessary quality standards and regulatory requirements.Key Responsibilities:Management of non-conformances, Technical writing abilities including, disposition, investigation/root cause analysis and implementing corrective actions.In-process product testing as needed.Follow up on Corrective Actions for in-process production NCs and customer complaint issues.Conduct area practice v's procedure audits and follow up on findings to ensure satisfactory closure.Experience with Good Manufacturing Practices (GMP) in a medical device-related industry is required.Support improvement of QMS documentation (i.e. Raise Change Requests, Write Procedures etc).Support validation activities including first article inspections as required.Support NPI/manufacturing operations area projects and initiatives e,g, Kaizen, yield improvement, cost reduction etcAdditional responsibilities as assigned by supervisor/managerEducation and Experience:Bachelor's degree in science, Quality, Engineering, Manufacturing, or related field is desirable but not essentialDecision-making ability while also working on one's initiative.Thorough knowledge of medical device quality systems.Must be innovative and be driven to implement changes to systems and procedures.Ability to Problem-solve including collecting data, establishing facts, and implementing actions.Must be able to communicate at all levels of the organisation and with customers, suppliers, and regulatory agencies.Excellent attention to detail.Excellent written and oral communication skills.Working knowledge of Microsoft Excel, Word, and PowerPoint General knowledge of commonly used measuring equipment and instrument selection.Working knowledge of calibration process.Ensuring compliance with applicable regulatory standards and internal GMP processes.