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Dessi Lyakov Location
San Diego, CA, US
Dessi Lyakov Work
Director Quality and Regulatory Affairs @ (August 2019 - Present)
Director Regulatory Affairs and Quality Assurance @ IRRAS USA, Inc. (May 2017 - August 2019)
Quality Assurance Engineer @ (November 2015 - May 2017)
Regulatory Affairs Director @ (January 2008 - August 2015)
QC and QA Manager @ Aalto Scientific, Ltd./AUDIT MicroControls (October 2003 - December 2007)
QC Analyst @ (November 2002 - September 2003)
Dessi Lyakov Education
University of Chemical Technology and Metallurgy, Sofia, Bulgaria
Master’s Degree (Chemical Engineering)
Dessi Lyakov Skills
CAPA
Corrective and Preventive Action (CAPA)
Design Control
FDA
GMP
Medical Devices
Quality Assurance
Quality Control
Quality System
R&D
Regulatory Affairs
SOP
Standard Operating Procedure (SOP)
U.S. Food and Drug Administration (FDA)
Validation
u.s. Food and Drug Administration Fda
Standard Operating Procedure Sop
Corrective and Preventive Action Capa
Microsoft Excel
Corrective and Preventive Action
u.s. Food and Drug Administration
Standard Operating Procedure
Dessi Lyakov Summary
Dessi Lyakov, based in San Diego, CA, US, is currently a Director Quality and Regulatory Affairs at CliniComp, Intl.. Dessi Lyakov brings experience from previous roles at IRRAS USA, Inc., Epic Sciences, Aalto Scientific, Ltd. and Aalto Scientific, Ltd./AUDIT MicroControls. Dessi Lyakov holds a Master’s Degree in Chemical Engineering @ University of Chemical Technology and Metallurgy, Sofia, Bulgaria. With a robust skill set that includes CAPA, Corrective and Preventive Action (CAPA), Design Control, FDA, GMP and more. Dessi Lyakov has 2 emails and 2 mobile phone numbers on RocketReach.
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