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GUNNAMSAIBABU@ YAHOO.CO.IN
+919490238210
1
GSB
OBJECTIVE
To associate with a
progressive
organization that
gives me scope to
update my
knowledge and skills
according to the
latest trends.
SKILLS
SOPSOPSOPSOP
DOCUMENTATION DOCUMENTATION DOCUMENTATION DOCUMENTATION CONTROLCONTROLCONTROLCONTROL
CAPA REVIEWCAPA REVIEWCAPA REVIEWCAPA REVIEW
OPERATE INSTRUMENTSOPERATE INSTRUMENTSOPERATE INSTRUMENTSOPERATE INSTRUMENTS
GUNNAM SAIBABU EXECUTIVE-QUALITY ASSURANCE
EXPERIENCE
EXECUTIVE – QA
STIRITI AYUR THERAPIES (P) LTD • FEB 2011 – TILL DATE
EXECUTIVE – QA
PHAARMASIA LTD • DEC 2008 TO JAN 2011
SR EXECUTIVE – QC
SS ORAL HYGIENE PRODUCTS (P) LTD • FEB 2001 TO NOV 2008
SUPERVISOR
VANTECH CHEMICALS (P) LTD • FEB 1997 TO FEB 2001
JOB RESPONSIBILITIES
• Handled instruments like HPLC, UV-Visible Spectrophotometer, Karl-
Fisher Apparatus, Refractometer, pH meter, Conductometer, Melting
Point Apparatus, and other lab equipments. Well versed with cGMP,
and GLP Standards pertaining to Pharma Industry.
• Analysis of raw materials, finished products (ie) parenterals well
versed with titrimetric analysis, instrumental analysis
• Responsible for the maintenance and review of calibrations,
instrument log books.
GSB GUNNAM SAIBABU EXECUTIVE-QUALITY ASSURANCE
GUNNAMSAIBABU@ YAHOO.CO.IN
+919490238210
2
INSTRUMENT INSTRUMENT INSTRUMENT INSTRUMENT VALIDATIONSVALIDATIONSVALIDATIONSVALIDATIONS
EQUIPMENT VALIDATIONEQUIPMENT VALIDATIONEQUIPMENT VALIDATIONEQUIPMENT VALIDATION
RAW MATERIAL ANALYSISRAW MATERIAL ANALYSISRAW MATERIAL ANALYSISRAW MATERIAL ANALYSIS
PROCESS CONTROLPROCESS CONTROLPROCESS CONTROLPROCESS CONTROL
INTERNAL AUDITSINTERNAL AUDITSINTERNAL AUDITSINTERNAL AUDITS
GMPGMPGMPGMP
• Monitoring in-process controls at various stages of manufacturing
• Investigations for Out-of-specification analysis, process and
procedural deviations and product failures with proper justification.
• Preparation, Review and approval of Standard Operating Procedures,
specifications, standard test procedures.
• Handling Deviations and Non-conformance activities
• Conducting regular internal audits.
• Preparation and Review of Standard Operating Procedures
• Good Manufacturing Practice Monitoring.
• Document Control and Issuance.
• Review of Filled BMRs and QC analytical reports.
• Cooperating in Handling of market complaints.
• Handling of Change controls and deviations.
EDUCATION
BSC • 1996 • ANDHRA UNIVERSITY
59%