Octavio Medina
About Octavio Medina
Octavio Medina serves as a Staff Quality Assurance Engineer at Biosense Webster, where he has worked since 2010. He holds an MBA from ITESM Campus Ciudad Juarez and has a background in Industrial Engineering, with extensive experience in project management and quality assurance in the medical device industry.
Work at BioSense Webster
Octavio Medina has been employed at BioSense Webster as a Staff Quality Assurance Engineer since 2010. In this role, he focuses on ensuring that products meet quality standards and regulatory requirements within the medical device industry. His tenure of 14 years reflects a commitment to maintaining high-quality practices and contributing to the overall success of the organization.
Education and Expertise
Octavio Medina holds a Master of Business Administration (MBA) from ITESM Campus Ciudad Juarez, which he completed in 2010. Prior to this, he earned a Bachelor's degree in Industrial Engineering from Instituto Tecnológico de Ciudad Juárez, studying from 1995 to 2002. His educational background supports his expertise in project management, particularly in capital and cost improvement initiatives.
Background in Project Management
Octavio Medina possesses a strong background in Capital and Cost Improvement Project Management. He has demonstrated skills in optimizing resources and reducing expenses, which are critical in the medical device sector. His experience in managing projects effectively contributes to the operational efficiency of the organizations he has worked with.
Leadership and Team Collaboration
Octavio has shown leadership in cross-functional teams within the medical device industry. His ability to collaborate across various departments highlights his skills in fostering teamwork and driving projects to successful completion. This experience is vital for ensuring that quality assurance processes are integrated throughout the organization.
Previous Experience in Quality Assurance
Before joining BioSense Webster, Octavio worked at Grayling Industries as an Engineering Manager from 2003 to 2010. He also served as a Quality Control Coordinator at Kimball International from 2000 to 2002. These roles provided him with extensive experience in quality assurance and internal auditing, essential for maintaining compliance and quality standards in the medical device sector.