Edgar Rodriguez-Vega

Edgar Rodriguez-Vega has a diverse range of work experience in the pharmaceutical industry. Edgar started their career in 2010 as a Manufacturing Process Technician at Amgen, where they gained knowledge of GMP and SOPs and utilized SAP to organize materials for manufacturing. Edgar then moved on to a role as a Sr. Mfg. Associate at Amgen, where they continued to expand their knowledge of SOPs and GMP areas, while also working in ISO6 areas and utilizing SAP, Werum, and LIMS for cataloging and organizing.

In 2017, Edgar became an Associate Scientist at Amgen, where they gained extensive knowledge in GMP areas, SOPs, and data interpretation. Edgar also led a pioneering project on a new database, PLM, and had experience with cell culture and purification processes.

Edgar then joined Bristol-Myers Squibb in 2018 as a Microbiologist, where they gained experience in Autoclave operation, environmental monitoring, and maintaining a 5S-oriented area.

In 2019, they became a Sr. Site Specialist at Thermo Fisher Scientific, where they were responsible for bioreactor assembly, cell culture sampling, and media and solution preparation. Edgar also had knowledge of CRIS, CisPro, and HLEE programs.

Currently, Edgar works as a Principal Manufacturing Specialist at Catalent Pharma Solutions. In this role, they focus on creating and reviewing procedures, preventing deviations, and leading audits. Edgar also has knowledge of deviation authoring and investigation.

Overall, Edgar Rodriguez-Vega has a strong background in manufacturing, GMP, SOPs, and data interpretation, with experience in multiple areas of the pharmaceutical industry.

From 2005 to 2010, Edgar Rodriguez-Vega pursued a Bachelor's degree in Microbiology, General at Universidad de Puerto Rico.