I am driven by my interest in analyzing manufacturing processes and identifying waste and process failure in order to implement continuous improvements. I have earned a reputation of diligent professional who can read reams of data to insure product compliance, safety and data accuracy. My most remarkable achievements to date include:- Reach a maintained a rate of 80% of non-conformity closed within 30 days.- Insured that 100% of compliant batches meet their expected release date according to company policies.- Identify and suggested 2 approved continuous improvement projects within the first 6 months of employment.My interests and inspirations include bioprocesses, Lean manufacturing, community building, transversal project management along with cooking, human rights and traveling. Specialities: - International cGMP- Manufacturing documentation lifecycle- Batch release- Non-conformance investigation- CAPA implementation- Continuous improvement- Validation- Scheduling- Risk analysis
Listed skills include Pharmaceutical Industry, Life Sciences, Validation, Capa, and 10 others.