An Industrial Engineer with a progressive track record in World Class Electronic and Medical Device manufacturing companies. Experience includes working and collaborating with people from diverse cultures and nationalities, while working in an FDA regulated environment. A Professional, pro-active, accountable individual that treats all issues with a high sense of urgency, that is results and goals oriented, with strong negotiation and assertive communication skills at all levels. An individual that values and embraces team work, problem solving while demonstrating leadership competencies at all times. An individual in search of joining an organization where continual improvement, meeting challenges and achieving Goals and Objectives are the expectations.

Business Analyst @ From October 2015 to Present (3 months) Regulatory Affairs and Quality Assurance Manager @ From December 2013 to August 2014 (9 months) Regulatory Affairs and Quality Assurance Specialist @ From April 2013 to November 2013 (8 months) CAPA, Complaints and Internal Audits Coordinator @ From May 2005 to April 2013 (8 years) Production Engineer @ From May 2000 to September 2003 (3 years 5 months)

Master of Business Administration (MBA), Industrial Engineering @ Instituto Tecnologico de Tijuana From 2008 to 2011 Industrial Engineering, with emphasis in Quality and Productivity @ Instituto Tecnologico de Tijuana From 1993 to 1998 Carmen Castillo is skilled in: CAPA, FDA, ISO 13485, Quality Assurance, Quality System, Quality Auditing, Root Cause Analysis, SPC, Medical Devices, ISO, GMP, V&V, Validation, ISO 14001, Internal Audit