Shailesh Tari

Postgraduate Master of Pharmacy (M.Pharm) in Quality Assurance with 20 years of experience in multinational pharmaceuticals. Expert in cGMP compliance, QC/QA, and regulatory audits (USFDA, MHRA, EU, WHO, ISO). Strong communication skills and proven track record in leading quality management teams across pharmaceutical manufacturing and contract manufacturing environments.

QA Manager - Amardeep Pharma Pvt Ltd - Tuem-Goa

(2025-04)

Reporting as Head-Quality to Plant Head & Managing Director

• Overall responsible for site compliance to cGMP & GLP
• Approval of all GMP related documents of site & new products registration
• Lead, direct & motivate the team to create strong quality culture
• Represent Internal / External audits of plant
• Ensure continuous improvement in QMS

AGM - QA - Meha Pharma Pvt Ltd - Kundaim-Goa

(2023-07 - 2025-04)

Reporting as Head-Quality to Managing Director

• Overall responsible for site compliance to cGMP & GLP
• Approval of all GMP related documents of site
• Lead, direct & motivate the team to create strong quality culture
• Represent Internal / External audits of plant
• Conduct RCA & implement CAPA to bring continuous improvement in QMS
• Ensure smooth functioning of all departments

Manager - Quality & Development - Goldy Finepacks Pvt Ltd - Kundaim-Goa

(2018-04 - 2023-07)

Reporting as Head-Q & D to Director Operations

• Implement & ensure compliance to cGMP & GLP
• Approval of quality documents such as SOPs, APQR, CC, Qualification & market complaints
• Create strong quality culture through trainings
• Represent Internal / External audit of plant and ensure CAPA compliance
• New product identification & development

Assistant Manager-QA - Awamedica Pharmaceuticals - Kurdistan

(2012-05 - 2017-04)

Reporting as Head-Quality to Plant Manager

• Approval of SMF, VMP and Quality/EHS manual
• Conduct self inspections of plant and follow up for CAPA compliance
• Approval of all Quality system Documents
• Represent and coordinate for internal & external Audits. eg Sanofi- Italy, ISO
• Conduct training on cGMP / GDP / Hygiene / GLP to all departments

Corporate QA- Executive - Indoco Remedies - India

(2011-03 - 2012-04)

Reporting to Manager-CQA

• Conduct RM, PM Vendor / Lab Audits in different locations of India
• Conduct self inspections and follow up for CAPA compliance
• Review quality systems such as Speciifcations, Deviations, Change controls & incidents
• Review of Process Validation, Qualification, APQR & market complaints

Pharmacist (MOH) - Saud Al-Jidaani Company - Saudi Arabia

(2008-05 - 2010-07)

Reporting to Managing Director

• Handling of MOH Inspections & Market Complaints
• Ensure Regulatory compliance as per MOH regulations
• Ensure pharmaceuticals are stored as per required storage condition

Research Scientist - ratiopharm R&D Ltd - Verna - Goa

(2005-08 - 2008-02)

Reporting to Asst. Manager

• Work in compliance with cGMP, GDP, GLP & regulatory agencies eg. ICH, WHO
• Perform Qualification (IQ/OQ/PQ) / Requalification of analytical Instruments
• Conduct Training based on SOPs, ICH & WHO cGMP guidelines for QA
• Analysis, Calibration & troubleshooting of analytical Instruments

Quality Control Supervisor - Ranbaxy Laboratories Ltd - Madcaim - Goa

(2002-03 - 2005-08)

Reporting to group leader

• Analysis of RM/ IP/ FP/ stability samples in compliance to GLP
• Preparation & compliance for regulatory audits: MHRA, WHO Audit

Master of Pharmacy - Quality Assurance - Goa University (2002-04)

Bachelor of Pharmacy - Goa University (2000-04)

Graduate Aptitude Test (Pharmaceutical) - Pharmaceutical - Indian Institute of Technology-Kharagpur (2000-03)

Higher Secondary School Certificate - Goa Board (1996-03)

Secondary School Certificate - Goa Board (1994-03)