---
title: "Mangesh Mawal - Sr. Manager Corporate Quality Assurance Manager in Bengaluru | Tal"
description: "Meet Mangesh Mawal, Sr. Manager CQA at Micro Labs Ltd. based in Bengaluru."
image: "https://tal.club/meet/mangesh-mawal/share-image"
---

# Mangesh Mawal on Tal

## Headline

Sr\. Manager CQA at Micro Labs Ltd\.

## About

Accomplished Quality & Compliance professional with 22\+ years of progressive experience across leading pharmaceutical companies\. Expertise in global regulatory compliance \(USFDA, MHRA, EU\-GMP, WHO, TGA\), audits, quality systems, and strategic quality leadership\. Proven success in leading cross\-border teams, global audits, and inspection readiness programs\. SME in QMS, QRM, Audit and compliance within different sector of QA \( R&D, Formulation and Corporate QA\)\. Successfully strengthen and keep improvise, the level of compliance at different organizations\. Mail ID : m\.mawal@rediffmail\.com

## Location

Bengaluru

## Work experience

Sr\. Manager Corporate Quality Assurance Manager at Micro Labs Ltd\., Nov 2017 \- Dec 2023 · 6 y 1 mo, India, As senior manager corporate, strengthen Corporate Quality Systems\. Improvise the state of compliance of manufacturing sites \(OSD & Ophthalmic\) and R&Ds\. Evaluate, improve Quality Systems to meet Regulatory Standards and Implementation of corporate remedial actions\. Responsible for GMP, GLP, monthely QSR presentation, QRM, Internal Audits and Management reviews compliances\. Responsible to ensure, integrity of data generated at formulation and analytical development\. Active role in trend Analysis of Quality System elements and identification of key improvement areas\. As Lead Auditor execution of Internal audits\. Ensure QMS compliances \(Change Management, Deviation Management, Lab Deviations/Incidents, Complaints Management, OOS/OOT and CAPA Management\)\. Formalize goals for team\. Mentor and improve quality resource knowledge/ skillsets of Individuals Responsible for onboard QMS, Monthly QSR, Risk Assessment through Product Life Cycle Approach and Quality trainings\. Accomplishments: Successfully play active role as Internal Lead auditor during Internal Audits\. Implemented QSR at corporate and R&D\. Extensive implementation of QRM from New Molecule to Product Life Cycle Approach\. Changed the mindset of the CFT from a reactive stance to proactive\. Drive improvements in KPI’s\. Trend analysis of SI observations and continuous training to Internal Auditors\.

Team Leader \- QA at Strides Shasun Limited, Apr 2012 \- Oct 2017 · 5 yrs 7 mos, India, As Team Leader Group Corporate Quality Assurance responsible for Compliance of manufacturing site and as development QA \(TSGQA\) responsible for compliance of development unit\. Handling of QMS through TW system, review and authorisation of MFR, MPR, PDP\-PDR\. Strides Arco Labs Apr 2012 \- 2017 As Team Leader Group Corporate Quality Assurance responsible for compliance of manufacturing site and as development QA \(TSGQA\) responsible for compliance of development unit\. Handling of QMS through TW system, review and authorization of MFR, MPR, PDP\-PDR\. Led Auditee for departmental audit and team auditor for plant internal audits\. Tracking trending of AQL data and implementation of actions\. Effective implementation of compliance monitoring tool i\.e\. CCTV and CP\-CCP log\. Identification of process, practice and procedural gaps and upgradation of system\. Analyzed data related to complaints, scrap, non\-conformances, and identification of additional controls Accomplishments Improved site quality compliance level to 100%\. Active contribution in USFDA & MHRA Audits\. Control process defect and obvious market complaints through continuous compliance review\. Ensure 100% procedural compliance from all department teams as well as eliminated data entry errors\. Trained and mentored Quality Team to lead internal compliance audits\.

Asst\. Manager Q\.A\. at Medreich Limited, Apr 2009 \- Apr 2012 · 3 yrs 1 mo, India, As Assistant Manager QA, responsible for Overall management of QMS \(Change Management, Deviation Management, Complaints Management and CAPA Management\)\. Responsible for Inspection Management \(Customer, regulatory and self\-inspection\), Risk Management, APQR and cleaning Validation\. Lead responsibility for compliance of audit non\-conformance and tracking for closure \(TGA, MHRA \(Twice\),WHO, customer audits like GSK India & Pfizer Global\) Responsible for investigation of customer complaints, audits, Process validations and Qualification activities\. Analyzed data related to Repetitive deviations, complaints, non\-conformances, and KPI’s to establish improvement plans\. Accomplishments Intime investigation of Market/Customer complaint with appropriate CAPAs\. Successful contribution and completion of MHRA and GSK Audits\. Reorganized the team responsibilities and improvise the induvial performance\. Key player in bringing QMS in state of compliance and online documentation\. Implement trend based analysis and assessment of to be implement/ implemented actions\.

Managment Staf \(QA \) at Cipla, Jun 2004 \- Mar 2009 · 4 yrs 10 mos, Kundaim \- Goa, As senior quality officer responsible for IPQA Activities and pack stock verification\. Handling of change control, deviation, market complaint and validation \(Process, cleaning and Non\-routine\)\. Review of water system, environmental trend and stability data\. Active role in site self\-inspection and audit preparation of other sites of Cipla\. In team role successfully evident USFDA, MHRA,WHO audits\. Accomplishments Major role in Audit preparation of Cipla units\. Intime execution of process validation, non\-routine validation and other documentation activities\.

Production QA at DALES REMEDIES PRIVATE LIMITED, Oct 2001 \- May 2004 · 2 yrs 8 mos, India, As FDA approved chemist responsible for, Manufacturing of external preparations \(Ointment,creams & lotions\)\. SOP preparation & review\. Audit & training\.

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