Sr. Director, Regulatory and Clinical Affairs @ (March 2020 - May 2024)
Manager, Regulatory Affairs @ (November 2019 - March 2020)
Manager, Regulatory Affairs and Quality Assurance @ (March 2017 - November 2019)
Manager, Regulatory Affairs @ Focus Diagnostics (Division of Quest Diagnostics) (December 2009 - February 2017)
Manager, Global Regulatory Affairs @ Alpine Biomed (Division of Natus Medical) (January 2009 - December 2009)
Regulatory Affairs Specialist @ Focus Diagnostics (Division of Quest Diagnostics) (March 2006 - December 2008)
Supervisor, Regulatory and Clinical Affairs @ Siemens Healthcare (formerly Diagnostics Products Corporation) (April 1996 - March 2006)
Roderick Castillo Education
UC Irvine
Bachelor of Science (BS) (Biology)
1992-1997
Conferences
Roderick Castillo Skills
FDA
ISO 13485
GMP
Medical Devices
Design Control
CAPA
Validation
Regulatory Affairs
Sop
V&V
Quality System
CE marking
ISO 14971
Change Control
Shipbuilding
Public Speaking
Telecom
Engineering
Management
Project Management
Pharmaceutical Industry
Capital
Roderick Castillo Summary
Roderick Castillo, based in Los Angeles, CA, US, is currently a Senior Director, Regulatory and Clinical Affairs at Siro Diagnostics. Roderick Castillo brings experience from previous roles at Cue Health Inc., FUJIFILM Irvine Scientific, TSK Laboratory and Focus Diagnostics (Division of Quest Diagnostics). Roderick Castillo holds a 1992 - 1997 Bachelor of Science (BS) in Biology @ UC Irvine. With a robust skill set that includes FDA, ISO 13485, GMP, Medical Devices, Design Control and more. Roderick Castillo has 1 emails and 3 mobile phone numbers on RocketReach.
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