Resumes
Resumes
President And Owner Of Fma Consulting, Llc
View pagePosition:
President-Owner at FMA Consulting, LLC
Location:
Houston, Texas
Industry:
Medical Devices
Work:
FMA Consulting, LLC - Houston, TX since Sep 2012
President-Owner
Millar Instruments, Inc. - Houston, Texas Area Jul 2008 - Aug 2012
Director of Quality and Regulatory Affairs
Cincinnati Sub-Zero Products Inc. - Cincinnati Area Jul 2007 - Jul 2008
Director of Quality and Regulatory Affairs
Delphi Medical Systems - Houston, Texas Area Jun 2004 - May 2007
Quality and Regulatory Affairs Manager/Senior Quality Engineer
Plastomer Technologies, EnPro Industries - Houston, Texas Area Aug 2000 - Jun 2004
Quality Manager
President-Owner
Millar Instruments, Inc. - Houston, Texas Area Jul 2008 - Aug 2012
Director of Quality and Regulatory Affairs
Cincinnati Sub-Zero Products Inc. - Cincinnati Area Jul 2007 - Jul 2008
Director of Quality and Regulatory Affairs
Delphi Medical Systems - Houston, Texas Area Jun 2004 - May 2007
Quality and Regulatory Affairs Manager/Senior Quality Engineer
Plastomer Technologies, EnPro Industries - Houston, Texas Area Aug 2000 - Jun 2004
Quality Manager
Education:
Delaware State University 1995 - 1996
Assiut University 1978 - 1982
BS, Electrical Engineering
Assiut University 1978 - 1982
BS, Electrical Engineering
Skills:
Medical Devices
ISO 13485
CAPA
QSR
Regulatory Affairs
Quality Assurance
Process Validation
Continuous Improvement
Regulatory Submissions
Design Control
Product Development
Compliance
Process Improvement
Lean Manufacturing
Biotechnology
CE marking
Risk Management
Process Engineering
Strategic Planning
FMEA
SPC
Problem Solving
Document Management
Process Development
cGMP practices
Medical Device-Clinical Evaluation
ISO 9001 Quality Management system
ASQ-Certified Quality Auditor
Quality System
V&V
Iso 9000
Quality Management
Process Simulation
Validation
ISO
FDA
GMP
Six Sigma
Engineering
Supplier Quality
Root Cause Analysis
Sop
Software Documentation
Quality Control
Change Control
ISO 13485
CAPA
QSR
Regulatory Affairs
Quality Assurance
Process Validation
Continuous Improvement
Regulatory Submissions
Design Control
Product Development
Compliance
Process Improvement
Lean Manufacturing
Biotechnology
CE marking
Risk Management
Process Engineering
Strategic Planning
FMEA
SPC
Problem Solving
Document Management
Process Development
cGMP practices
Medical Device-Clinical Evaluation
ISO 9001 Quality Management system
ASQ-Certified Quality Auditor
Quality System
V&V
Iso 9000
Quality Management
Process Simulation
Validation
ISO
FDA
GMP
Six Sigma
Engineering
Supplier Quality
Root Cause Analysis
Sop
Software Documentation
Quality Control
Change Control
Interests:
medical device opportunities in quality and regulatory consulting.