Personal Information
Unternehmen/Arbeitsplatz
Ahmedabad Area, India India
Branche
Medical / Health Care / Pharmaceuticals
Info
Trained and carrier-oriented Quality Professional presently engaged at Quality Assurance, with Reputed Pharmaceutical industry, Ahmedabad.
Has a unique and comprehensive experience in Veterinary & Human Vaccine manufacturing and Parenteral Dosage manufacturing, project management arenas and excellent technical and practical knowledge of various Validation and Qualification activities. Brief as Autoclave, DHS, HVAC, Tunnel, Lyophillizer, Change management in ISO and GMP with high efficiency in CAPA. Documentation,
Quality Management in vaccine & parenteral manufacturing, process and cleaning validation, QbD, QRM, SOP’s, cGMP, GLP,USFDA, EU, ISO 9000 and ISO 14001, ISO 45001.
Tags
methane
alkane
oos
pharmaceutical validation
validation
qualification
risk score
quality risk management
qrm
risk
good manufacturing practices
cgmp
gmp
particles
contamination
cleanroom
good aseptic practices
aseptic
metadata
di
data integrity
sterility
sterility failure
sterility failure investigation.
butane
propane
ethane
hiv
aids
haydrocabon
reaction
solvent
quantum mechanics
molecularmodelling
computational chemistry
quality assurance
qa
sampling
sampling plan
sample
out of specification
continous improvement
deviation
pharmaceutical process validation
process validation
gdp
documentation
change control
cc
standarad operating procedure
sop
good documentation practice
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(2)DATA INTEGRITY GMP COMPLIANCE
Pharmaceutical
•
Vor 5 Jahren
Good documentation practice
Pharmaceutical
•
Vor 11 Jahren
Personal Information
Unternehmen/Arbeitsplatz
Ahmedabad Area, India India
Branche
Medical / Health Care / Pharmaceuticals
Info
Trained and carrier-oriented Quality Professional presently engaged at Quality Assurance, with Reputed Pharmaceutical industry, Ahmedabad.
Has a unique and comprehensive experience in Veterinary & Human Vaccine manufacturing and Parenteral Dosage manufacturing, project management arenas and excellent technical and practical knowledge of various Validation and Qualification activities. Brief as Autoclave, DHS, HVAC, Tunnel, Lyophillizer, Change management in ISO and GMP with high efficiency in CAPA. Documentation,
Quality Management in vaccine & parenteral manufacturing, process and cleaning validation, QbD, QRM, SOP’s, cGMP, GLP,USFDA, EU, ISO 9000 and ISO 14001, ISO 45001.
Tags
methane
alkane
oos
pharmaceutical validation
validation
qualification
risk score
quality risk management
qrm
risk
good manufacturing practices
cgmp
gmp
particles
contamination
cleanroom
good aseptic practices
aseptic
metadata
di
data integrity
sterility
sterility failure
sterility failure investigation.
butane
propane
ethane
hiv
aids
haydrocabon
reaction
solvent
quantum mechanics
molecularmodelling
computational chemistry
quality assurance
qa
sampling
sampling plan
sample
out of specification
continous improvement
deviation
pharmaceutical process validation
process validation
gdp
documentation
change control
cc
standarad operating procedure
sop
good documentation practice
Mehr anzeigen