Harry Lorenzo
About Harry Lorenzo
Harry Lorenzo is a Senior Packaging Technology Specialist at Bristol-Myers Squibb in New York, with extensive experience in validation engineering and a diverse background in various engineering roles within the medical device industry.
Title
Harry Lorenzo serves as the Senior Packaging Technology Specialist at Bristol-Myers Squibb in New York, New York, United States. In this role, he brings substantial experience in validation engineering and packaging technology to enhance the company's packaging solutions.
Company
Harry Lorenzo is currently employed at Bristol-Myers Squibb, a global biopharmaceutical company. He has been with the organization for over 8 years, starting in September 2015. At Bristol-Myers Squibb, he focuses on advanced packaging technology crucial for the safe delivery of pharmaceutical products.
Education and Expertise
Harry Lorenzo holds two bachelor's degrees. He earned a Bachelor of Arts from the University of Puerto Rico, Mayagüez Campus, from 1998 to 2002. Subsequently, he completed a bachelor's degree from the Universidad Politécnica de Puerto Rico between 2002 and 2006. His academic background laid the foundation for his diverse expertise in validation engineering, packaging technology, and project management in the medical device and pharmaceutical industries.
Background
Harry Lorenzo has a diverse engineering background with experience in various roles across multiple companies. He began his career at B. Braun Group as Project Support in 2006, then moved to Infotech Aerospace Services, Inc. as a Project Specialist from 2007 to 2010. Following this, he worked at Edwards Lifesciences as a Manufacturing Engineer from 2010 to 2012 and later as a Validation Engineer in 2013. He also held roles such as Quality Engineer at St. Jude Medical in 2013, Validation Engineer at Baxter International Inc. from 2012 to 2013, and Validation Specialist at Zimmer Biomet from 2014 to 2015.
Experience in Medical Device Industry
Harry Lorenzo has extensive experience in the medical device industry. He worked at Edwards Lifesciences, St. Jude Medical, and Baxter International Inc., holding positions that ranged from Manufacturing Engineer to Quality Engineer and Validation Engineer. His roles in these organizations involved ensuring compliance with regulatory standards and improving product quality and manufacturing processes.