Surya Kesanapalli
14+ years of experience in (Process, CSV, Cleaning, and Equipment Validation) and Quality Assurance in the Software... | Santa Monica, California, United States
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Surya Kesanapalli’s Emails sk****@ki****.com
Surya Kesanapalli’s Phone Numbers No phone number available.
Social Media
Surya Kesanapalli’s Location Santa Monica, California, United States
Surya Kesanapalli’s Expertise 14+ years of experience in (Process, CSV, Cleaning, and Equipment Validation) and Quality Assurance in the Software and Pharma industries. Computer system validation inspection involves IQ, OQ, and PQ (Installation, Operation and Performance Qualification) Vendor and supplier evaluation LEAN SIX SIGMA EDMS, EQMS, LMS ( Electronic Data Management System, Electronic Quality Management System, Learning Management System) Guideline Regulatory expertise in OECD, EU MDA, ICH -Q4, Q6, Q9, ISO 9001:1025, ISO 13485, ISO14971, US FDA, 21 CFR Part 11, 21, 150, USP, MHRA, EMA Approvals, EU approvals and Schedule Y. Specialized Areas: - CSV Verification and Validation - Equipment Validation, Cleaning Validation - Pre-clinical toxicology - Genotoxicology - Viral clearance testing - Biological sample testing - Analytical - Bio-analytical sample testing - Labware - Cancer Biology - Six Sigma - Regulatory guidelines - 21 CFR P11, USFDA, Annexure-11, ISO-10993, ISO-9001, EU, MDR - Medical devices, and - Regulatory Affairs
Surya Kesanapalli’s Current Industry Kite Pharma
Surya
Kesanapalli’s Prior Industry
Sugen Life Sciences
|
Syngene International
|
Mindtree
|
Philips
|
Kite Pharma
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Work Experience
Kite Pharma
Validation Lead
Sat Jul 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Present
Philips
Sr. Quality Test Engineer - Csv
Sat Apr 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Jun 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Mindtree
Software Validation Engineer
Thu Apr 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Apr 01 2023 00:00:00 GMT+0000 (Coordinated Universal Time)
Syngene International
Assistant Manager - Validation Test Specialist (Csv)
Fri Jun 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)
Syngene International
Test Specialist (Equipment Validation)
Tue Sep 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jun 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time)
Sugen Life Sciences
Verification & Validation Lead (V&V)
Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time) — Sat Feb 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)
Sugen Life Sciences
Equipment Validation Engineer
Sat Aug 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Jun 01 2010 00:00:00 GMT+0000 (Coordinated Universal Time)
Sugen Life Sciences
Equipment / Cleaning Validation Engineer
Thu May 01 2008 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Jul 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)Skills
Languages
Surya Kesanapalli Email Addresses
FAQ About Surya Kesanapalli
-
Surya Kesanapalli is located at
Santa Monica, California, United States -
Surya Kesanapalli is a
14+ years of experience in (Process, CSV, Cleaning, and Equipment Validation) and Quality Assurance in the Software and Pharma industries. Computer system validation inspection involves IQ, OQ, and PQ (Installation, Operation and Performance Qualification) Vendor and supplier evaluation LEAN SIX SIGMA EDMS, EQMS, LMS ( Electronic Data Management System, Electronic Quality Management System, Learning Management System) Guideline Regulatory expertise in OECD, EU MDA, ICH -Q4, Q6, Q9, ISO 9001:1025, ISO 13485, ISO14971, US FDA, 21 CFR Part 11, 21, 150, USP, MHRA, EMA Approvals, EU approvals and Schedule Y. Specialized Areas: - CSV Verification and Validation - Equipment Validation, Cleaning Validation - Pre-clinical toxicology - Genotoxicology - Viral clearance testing - Biological sample testing - Analytical - Bio-analytical sample testing - Labware - Cancer Biology - Six Sigma - Regulatory guidelines - 21 CFR P11, USFDA, Annexure-11, ISO-10993, ISO-9001, EU, MDR - Medical devices, and - Regulatory Affairs Kite Pharma -
Surya Kesanapalli currently works in the
Kite Pharma -
Surya Kesanapalli specializes in
14+ years of experience in (Process, CSV, Cleaning, and Equipment Validation) and Quality Assurance in the Software and Pharma industries. Computer system validation inspection involves IQ, OQ, and PQ (Installation, Operation and Performance Qualification) Vendor and supplier evaluation LEAN SIX SIGMA EDMS, EQMS, LMS ( Electronic Data Management System, Electronic Quality Management System, Learning Management System) Guideline Regulatory expertise in OECD, EU MDA, ICH -Q4, Q6, Q9, ISO 9001:1025, ISO 13485, ISO14971, US FDA, 21 CFR Part 11, 21, 150, USP, MHRA, EMA Approvals, EU approvals and Schedule Y. Specialized Areas: - CSV Verification and Validation - Equipment Validation, Cleaning Validation - Pre-clinical toxicology - Genotoxicology - Viral clearance testing - Biological sample testing - Analytical - Bio-analytical sample testing - Labware - Cancer Biology - Six Sigma - Regulatory guidelines - 21 CFR P11, USFDA, Annexure-11, ISO-10993, ISO-9001, EU, MDR - Medical devices, and - Regulatory Affairs -
Surya Kesanapalli speaks the following languages:
No languages available. -
Surya Kesanapalli has prior experience in the following industries:
Philips , Mindtree , Syngene International , Syngene International , Sugen Life Sciences , Sugen Life Sciences , Sugen Life Sciences -
Surya Kesanapalli has the following professional experience:
Kite Pharma , Philips , Mindtree , Syngene International , Syngene International , Sugen Life Sciences , Sugen Life Sciences , Sugen Life Sciences . -
You can view Surya Kesanapalli’s
LinkedIn profile at LinkedIn URL. -
Surya Kesanapalli’s work email addresses are
[email protected] . -
Surya Kesanapalli works at
Kite Pharma
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