Personal Information
Organización/Lugar de trabajo
Bangladesh Bangladesh
Ocupación
Head of Quality Unit
Sector
Medical / Health Care / Pharmaceuticals
Sitio web
gmp-geek.weebly.com/
Acerca de
A pharmaceutical and biopharmaceutical professional with 12 years of practical expertise in the development, integration, management, and improvement of quality management systems for GMP and technical processes. Having a thorough understanding of how quality systems can govern and improve lean, efficient, and productive GMP operations. Successive increases in responsibilities and multi-disciplinary duties allow me to have a broad perspective of manufacturing capabilities, global compliance standards, and how to integrate the two within an efficient and effective Quality System.
Etiquetas
md saddam nawaz
pharmaceuticals
fda
ich
ep
bp
usp
method validation
method development
quality risk management
quality by design
q10
q9
q8
pharmaceutical process validation
21 cfr
r&d
ich q2
technology transfer
pat
quality management
good manufacturing practice
gmp
linearity
precision
accuracy
particle size distribution analyzer
usp 1092
dissolution
fmea
fta
cpp
cqa
life cycle
drugs
ema
pharmaceutical development
quality
qualification
validation
continued process verification
verification
eu annex 15
ispe
astm e2500
pharmaceutical
qualification and validation
equipment
utility
facility
Ver más
Presentaciones
(5)Personal Information
Organización/Lugar de trabajo
Bangladesh Bangladesh
Ocupación
Head of Quality Unit
Sector
Medical / Health Care / Pharmaceuticals
Sitio web
gmp-geek.weebly.com/
Acerca de
A pharmaceutical and biopharmaceutical professional with 12 years of practical expertise in the development, integration, management, and improvement of quality management systems for GMP and technical processes. Having a thorough understanding of how quality systems can govern and improve lean, efficient, and productive GMP operations. Successive increases in responsibilities and multi-disciplinary duties allow me to have a broad perspective of manufacturing capabilities, global compliance standards, and how to integrate the two within an efficient and effective Quality System.
Etiquetas
md saddam nawaz
pharmaceuticals
fda
ich
ep
bp
usp
method validation
method development
quality risk management
quality by design
q10
q9
q8
pharmaceutical process validation
21 cfr
r&d
ich q2
technology transfer
pat
quality management
good manufacturing practice
gmp
linearity
precision
accuracy
particle size distribution analyzer
usp 1092
dissolution
fmea
fta
cpp
cqa
life cycle
drugs
ema
pharmaceutical development
quality
qualification
validation
continued process verification
verification
eu annex 15
ispe
astm e2500
pharmaceutical
qualification and validation
equipment
utility
facility
Ver más