Resumes
Resumes
Seeking A Full Time Ra/Qa Position In Pharmaceutical, Biotechnology Or Medical Devices Industry.
View pageLocation:
Greater Los Angeles Area
Industry:
Medical Devices
Work:
Posey Company Aug 2012 - Nov 2012
RA/QA Specialist
PSC Biotech - Pomona, CA Jan 2012 - Jul 2012
QA Engineer
Neutrogena - Greater Los Angeles Area Mar 2012 - May 2012
Regulatory Affairs/Quality Engineer
University of Southern California - Greater Los Angeles Area Nov 2009 - Dec 2011
QA Supervisor
Garle Impex - New Delhi Area, India Aug 2008 - Jul 2009
Biomedical Engineer
RA/QA Specialist
PSC Biotech - Pomona, CA Jan 2012 - Jul 2012
QA Engineer
Neutrogena - Greater Los Angeles Area Mar 2012 - May 2012
Regulatory Affairs/Quality Engineer
University of Southern California - Greater Los Angeles Area Nov 2009 - Dec 2011
QA Supervisor
Garle Impex - New Delhi Area, India Aug 2008 - Jul 2009
Biomedical Engineer
Education:
University of Southern California 2009 - 2012
Masters in Engineering, Biomedical Engineering I.E.T. Bundelkhand University 2004 - 2008
B.Tech, Biotechnology Engineering
Masters in Engineering, Biomedical Engineering I.E.T. Bundelkhand University 2004 - 2008
B.Tech, Biotechnology Engineering
Skills:
Quality System
Root Cause Analysis
Medical Devices
FMEA
ELISA
PCR
Matlab
Cell Culture
ISO 13485
GMP
FDA
Western Blotting
Chromatography
C
Six Sigma
Design Control
ISO 14971
Sop
CAPA
Validation
Biomedical Engineering
Quality Assurance
Minitab
Regulatory Affairs
Quality Control
21 CFR Part 11
PMA
V
GLP
SDS-PAGE
Biotechnology
Lifesciences
LIMS
Technology Transfer
Medical Device Directive
FDA GMP
Quality Auditing
Regulatory Submissions
HPLC
Change Control
Sterilization
Complaint Management
GCP
Computer System Validation
Regulatory Requirements
Root Cause Analysis
Medical Devices
FMEA
ELISA
PCR
Matlab
Cell Culture
ISO 13485
GMP
FDA
Western Blotting
Chromatography
C
Six Sigma
Design Control
ISO 14971
Sop
CAPA
Validation
Biomedical Engineering
Quality Assurance
Minitab
Regulatory Affairs
Quality Control
21 CFR Part 11
PMA
V
GLP
SDS-PAGE
Biotechnology
Lifesciences
LIMS
Technology Transfer
Medical Device Directive
FDA GMP
Quality Auditing
Regulatory Submissions
HPLC
Change Control
Sterilization
Complaint Management
GCP
Computer System Validation
Regulatory Requirements
Certifications:
ISO 13485:2003 Internal Quality Auditor
Understanding Patents & Patent Application Process for Engineers & Scientists, Research Commercialization & SBIR Center
Total Quality Management Certification
Understanding Patents & Patent Application Process for Engineers & Scientists, Research Commercialization & SBIR Center
Total Quality Management Certification
Ashish Yadav
View pageLocation:
United States
Seeking A Full Time Ra/Qa Position In Pharmaceutical, Biotechnology Or Medical Devices Industry.
View pageLocation:
Greater Los Angeles Area
Industry:
Medical Devices
Ashish Yadav
View pageLocation:
United States
Ashish Yadav
View pageLocation:
United States
Ashish Yadav
View pageLocation:
United States
Ashish Yadav
View pageLocation:
United States
Ashish Yadav
View pageLocation:
United States