3 years working experience in latex based medical device industry. Heavily involved in Continuous Improvement Projects, Process Control activities, Root Cause Analysis. Current job scope include performing engineering studies, executing validations (OQ,PQ), and co-lead root cause analysis using DMAIC approach. Well versed in medical device documentations such as drafting protocols, report, and CAPA documentation. Currently enrolled in Lean Practitioner certification. High interest in continuous improvement projects.