| Resume alert | Resumes 61 - 68 of 68 |
DCS & instrumentation enginers with 6 + years of experience in Industd
Bangalore, KA, 560019, India
... based Electronic signature for all control loops for Experion MX 1 Project Scope: Electronic signature for control loops Project to comply with Honeywell Experion MX product with 21CFR FDA rule for pharmaceutical industry and certify for the same. ... - 2013 Feb 13
... based Electronic signature for all control loops for Experion MX 1 Project Scope: Electronic signature for control loops Project to comply with Honeywell Experion MX product with 21CFR FDA rule for pharmaceutical industry and certify for the same. ... - 2013 Feb 13
Medical Device Management
Bangalore, KA, India
... Standards familiar with: o Risk Analysis: ISO 14971 o ISO 13485:2003, ISO 9001: 2008 o Medical device regulation of FDA, European (CE), Indian medical device regulations PROjects . Out-Patient-Department Process Simulation of a Tertiary Care Super ... - 2012 Dec 28
... Standards familiar with: o Risk Analysis: ISO 14971 o ISO 13485:2003, ISO 9001: 2008 o Medical device regulation of FDA, European (CE), Indian medical device regulations PROjects . Out-Patient-Department Process Simulation of a Tertiary Care Super ... - 2012 Dec 28
Resume
Bangalore, KA, 562123, India
... AUDIT FACED • MHRA • WHO • EDQM • FDA AUDIT FACED (CUSTOMER) • J&J • GSK • Merck • Novartis • Cipla VALIDATION • Sterility test validation of product. • Bacterial endotoxin Test validation of product. • Dry heat sterilizer validation. • Water ... - 2012 Nov 26
... AUDIT FACED • MHRA • WHO • EDQM • FDA AUDIT FACED (CUSTOMER) • J&J • GSK • Merck • Novartis • Cipla VALIDATION • Sterility test validation of product. • Bacterial endotoxin Test validation of product. • Dry heat sterilizer validation. • Water ... - 2012 Nov 26
Pvt Ltd Executive
Bangalore, KA, 560067, India
... I handled US FDA audit in cipla . . I handled internal audits as an auditor for ISO 9001&22000. . Optimum utilization of man power and equipments. . Creating pleasant working condition by maintaining good house keeping and discipline. . Monitoring ... - 2012 Nov 14
... I handled US FDA audit in cipla . . I handled internal audits as an auditor for ISO 9001&22000. . Optimum utilization of man power and equipments. . Creating pleasant working condition by maintaining good house keeping and discipline. . Monitoring ... - 2012 Nov 14
Medical Manager
Bangalore, KA, 560102, India
... • FDA guidelines for the development of the” Gene Expression Profiling Test System for • Breast Cancer Prognosis”, at R&D centre, Avesthagen Ltd • FDA guidelines for the development of In-vitro diagnostic kit, at R&D centre, Avesthagen Ltd. HANDS ON ... - 2012 Oct 30
... • FDA guidelines for the development of the” Gene Expression Profiling Test System for • Breast Cancer Prognosis”, at R&D centre, Avesthagen Ltd • FDA guidelines for the development of In-vitro diagnostic kit, at R&D centre, Avesthagen Ltd. HANDS ON ... - 2012 Oct 30
Manager Training
Bangalore, KA, 560094, India
... and validation, study sample analysis using different assay formats such as, ELISA, ECL (MSD), CLIA, SPR, RIPA/RIA assays and Cell based assays for PK and Immunogenicity assessment under GLP /GCLP compliant practices for EMEA and US FDA submissions. ... - 2012 Oct 02
... and validation, study sample analysis using different assay formats such as, ELISA, ECL (MSD), CLIA, SPR, RIPA/RIA assays and Cell based assays for PK and Immunogenicity assessment under GLP /GCLP compliant practices for EMEA and US FDA submissions. ... - 2012 Oct 02
Quality Assurance Management
Bengaluru, India
... (FDA, EU, ANVISA) Carried out review of clinical documents for accuracy & completion (IRB/IEC Approval, Investigator’s undertaking). Monitored General and Study specific screening procedures for Recruitment, Enrollment of volunteers and the process ... - 2011 Feb 04
... (FDA, EU, ANVISA) Carried out review of clinical documents for accuracy & completion (IRB/IEC Approval, Investigator’s undertaking). Monitored General and Study specific screening procedures for Recruitment, Enrollment of volunteers and the process ... - 2011 Feb 04
Sr. Project Manager
Banglore, KA, 560016, India
... If any drug causes any adverse reaction then it needs to be reported to authorities like MHLW, FDA etc within a specified time period depending upon the severity of adverse reaction. There are many other related products owned by Arisglobal like ... - 2010 Jul 02
... If any drug causes any adverse reaction then it needs to be reported to authorities like MHLW, FDA etc within a specified time period depending upon the severity of adverse reaction. There are many other related products owned by Arisglobal like ... - 2010 Jul 02