---
title: "Rajesh Surada - Deputy Manager in Hyderabad | Tal"
description: "Meet Rajesh Surada, Deputy Manager, Biotechnology, Upstream Cell culture Manufacturing, MSAT, Process Validation, Qualification, Quality Management System, Computer System Validation & Computer System Assurance, ISO 9001:2015&ISO 13485:2016 based in Hyderabad."
image: "https://tal.club/meet/rajesh-14/share-image"
---

# Rajesh Surada on Tal

## Headline

Deputy Manager, Biotechnology, Upstream Cell culture Manufacturing, MSAT, Process Validation, Qualification, Quality Management System, Computer System Validation &amp; Computer System Assurance, ISO 9001:2015&amp;ISO 13485:2016

## About

Biopharmaceutical Upstream SME with 11\+ years in GMP and Automation Systems

## Location

Hyderabad

## Work experience

Deputy Manager at SUN PHARMA, Oct 2022 \- Jul 2024 · 1 yr 10 mos, India, • Executed DeltaV\-controlled automated single\-use bioreactor batches in validated GMP environment • Monitored SCADA alarms, interlocks, and process trends during batch execution • Lead process validation and CPV trending for automated batches • Managed deviations, CAPA, Gap and Risk assessments related to process and facility • Supported change control activities impacting DeltaV\-controlled automated workflows • Collaborated with QA and CSV teams for validation of eQMS systems, including documentation review and execution support

Process Lead at Kemwell Biopharma, Sep 2020 \- Mar 2022 · 1 yr 7 mos, Bengaluru, Karnataka, India, • Executed 2000L stainless steel bioreactor campaigns using Wonderware automation systems • Monitored CPP trends using historian data and supported process optimization • Supported equipment qualification and validation documentation review • Managed deviation investigations and Change control activities • Delivered training through ComplianceWire eLMS platform

Junior Manager at Syngene International Limited, Dec 2018 \- Aug 2020 · 1 yr 9 mos, Greater Bengaluru Area, • Executed automated seed train and production bioreactor operations using DeltaV systems\. • Managed deviation investigations and change control using TrackWise eQMS • Collaborated with CSV teams on validation documentation and system compliance activities

Assistant Manager at Dr\. Reddy's Laboratories, Sep 2014 \- Dec 2018 · 4 yrs 4 mos, Hyderabad, Telangana, India, • Executed upstream manufacturing using automated stainless\-steel bioreactors • Monitored critical process parameters \(pH, DO, gas flow\) using PI historian • Supported process validation and SAP\-based batch documentation activities • Authored SOPs and BMRs aligned with GMP requirements • Participated in equipment qualification \(IQ/OQ/PQ\) and validation activities

Jr\.Executive at Kemwell Biopharma, Oct 2012 \- Aug 2014 · 1 yr 11 mos, On\-site, • Authored and executed IQ/OQ/PQ protocols for upstream process equipment • Prepared URS, RTM, and validation documentation for DS facility equipment • Participated in FAT/SAT and media simulation activities for upstream readiness

## Education

Master's degree, Biotechnology, Sathyabama University Dental College And Hospital

Bachelor's degree, Biotechnology, kl university

[View the original profile](https://tal.club/meet/rajesh-14)

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