Benjamin Nelson
About Benjamin Nelson
Benjamin Nelson is a Senior Manufacturing Engineer at Boston Scientific with extensive experience in the pharmaceutical and manufacturing industries.
Title: Sr. Manufacturing Engineer at Boston Scientific
Benjamin Nelson holds the position of Sr. Manufacturing Engineer at Boston Scientific. He has been employed there since 2019. His role involves overseeing manufacturing processes, ensuring efficiency and compliance with industry standards, particularly U.S. Title 21 CFR Part 11. This position builds on his extensive background in engineering and automation, providing a critical backbone to the company's manufacturing operations.
Previous Positions: Pfizer and Global Validation Solutions
Prior to his current role, Benjamin Nelson worked at Pfizer, starting as a Process Engineer from 2011 to 2014 based in Guayama, Puerto Rico, and then as an Automation Specialist from 2014 to 2019. His responsibilities included process optimization and implementing automated solutions to improve manufacturing workflows. Before his tenure at Pfizer, he served as a Validation Specialist at Global Validation Solutions, Inc. from 2004 to 2009 in Canovanas, Puerto Rico, where he focused on ensuring that systems and processes met regulatory requirements.
Education: Engineering and Business Administration
Benjamin Nelson has a robust educational background with multiple degrees. He earned a Bachelor’s degree in Electrical and Electronics Engineering from the University of Puerto Rico-Mayaguez in 2002. He later achieved a Master of Business Administration focused on Operations Management from the University of Puerto Rico, Río Piedras in 2008, which provided him with invaluable knowledge in managing manufacturing operations. Additionally, he holds a Master of Science in Electrical and Electronics Engineering from Boston University, attained in 2010, enhancing his technical expertise in automation.
Expertise: Compliance and Quality in Manufacturing
Benjamin Nelson brings significant expertise in areas critical to the pharmaceutical and manufacturing sectors. He is well-versed in U.S. Title 21 CFR Part 11 Regulation, which is essential for regulatory compliance in the pharmaceutical industry. His skill set also includes Corrective and Preventive Action (CAPA), crucial for maintaining the quality and compliance of manufacturing processes. These competencies ensure that his contributions effectively support the stringent quality standards required in the industry.