Personal Information
Organization / Workplace
Mumbai Area, India India
Occupation
Quality Manager, Pharmaceutical GMP Professional & Quality Auditor
Industry
Medical / Health Care / Pharmaceuticals
Website
seetharamkandarpa.webnode.in/
About
Over 15 years of versatile, industrial experience in various functions like Corporate QA/ Site QA/ Global Quality Management / Production for API and Formulation facilities (approved by various regulatory agencies USFDA, TGA, MHRA, WHO etc.) of top pharma companies in India.
Wide experience in complying various cGMP regulations/ standards such as 21 CFR, ICH, WHO guidelines, EMA regulations, PIC/S, EU-GMP, Canada GMP, TGA GMP, ISO 9001, ISO14001, ISO 19011 etc.
Well versed in design of various types of quality management system documentation such as quality manual, SOPs, work instructions, site master file, corporate guidance documents, employee training program, vendor management
Tags
seetharam kandarpa
asq
iso 19011
audit
certification
cpgp
cqa
gmp
usfda
ich
management systems
iso 19011:2018
guideline
standard
auditing fundamentals
american society for quality
certificed quality auditor
seettharam kandarpa
srk
certified pharmaceutical gmp professional
auditor
quality
asq cqa
quality risk management
q9
health canada
who
mhra
pdca
deming
internal quality audit
qbd
q10
iso 9001
pharmaceutical quality system
See more
Presentations
(7)Likes
(5)Professional Development: A Gap Between Bench 2 Bedside
Ajaz Hussain
•
6 years ago
A platform for assurance & efficiency - Ajaz at USP PCM Mumbai 2017
Ajaz Hussain
•
7 years ago
ISO 9001 2015 Overview presentation
Govind Ramu
•
8 years ago
US FDA Process Validation Stage 2 : No. Of Batches Required for Process Performance Qualification.
GMP EDUCATION : Not for Profit Organization
•
8 years ago
Personal Information
Organization / Workplace
Mumbai Area, India India
Occupation
Quality Manager, Pharmaceutical GMP Professional & Quality Auditor
Industry
Medical / Health Care / Pharmaceuticals
Website
seetharamkandarpa.webnode.in/
About
Over 15 years of versatile, industrial experience in various functions like Corporate QA/ Site QA/ Global Quality Management / Production for API and Formulation facilities (approved by various regulatory agencies USFDA, TGA, MHRA, WHO etc.) of top pharma companies in India.
Wide experience in complying various cGMP regulations/ standards such as 21 CFR, ICH, WHO guidelines, EMA regulations, PIC/S, EU-GMP, Canada GMP, TGA GMP, ISO 9001, ISO14001, ISO 19011 etc.
Well versed in design of various types of quality management system documentation such as quality manual, SOPs, work instructions, site master file, corporate guidance documents, employee training program, vendor management
Tags
seetharam kandarpa
asq
iso 19011
audit
certification
cpgp
cqa
gmp
usfda
ich
management systems
iso 19011:2018
guideline
standard
auditing fundamentals
american society for quality
certificed quality auditor
seettharam kandarpa
srk
certified pharmaceutical gmp professional
auditor
quality
asq cqa
quality risk management
q9
health canada
who
mhra
pdca
deming
internal quality audit
qbd
q10
iso 9001
pharmaceutical quality system
See more