Highlights:A chemical engineering graduate with Continuous professional development attitude having multiple certifications and courses ,Having roots to constant learning and adaptation. Contributing towards better health of society with my knowledge,skills and extensive experience of 5.5 years in Pharmaceutical quality operatiins.

Skills:LIMS, SAP, HPLC, GC, AAS, FTIR, QMS, HSE, Chromatography, Laboratory, OOS, Root cause analysis, OOT, R&D, New product development, Stability studies, USP,BP,EP, Pharmacopoeias, ICH,WHO,USFDA guidelines, Risk assesement, ISO 9001 Lead auditor, Titration, Validation, CAPA, Deviation, Change control, Data integrity, ALCOA +, cGMP, GLP, Laboratory safety, TOC, UV, 21 CFR part 11, Verification, Calibration, IQ,OQ,PQ, Method validation, Cleaning validation, titrimetry, spectroscopy

Goal:To enhance my professional skills in a dynamic and stable workplace.contribute with my experience and expertise which productive in all dimensions aligned with employers vision and play my role for betterment and well being of society

Membership:American institute of chemical engineers, Oshatrain, Unincef, WHO online USP learning

Certification:ISO 9001 QMS Lead auditor Lean six sigma foundation course Lab safety First Aid ,Cpr Aed CSWL level 2 Gemba kaizen 5s workplace productivity Sustainble strategies Quality Risk management Root cause analysis Auditing Industry 4.0 Emergency preparedness and response Foundations of digital marketting

Honor:Designated as SME (Subject matter expert) for Raw materials and Stability chambers in WHO prequalification ? Introducing sustainability concept in QC ? Handling regulatory bodies query in export requirements ? Installation and commissioning of Lab equipment’s mainly GC MS and potentiometer autotitrator ? New vendor development of lab chemicals ? Initiating safety audits in Laboratory ? Contributing towards goal of “zero waste policy” by suggesting solvent recovery system

Executive quality control 02/2021 - current
Aspin pharmaceutical (formerly johnson n johnson pakistan), Karachi, sindh Pakistan
Industry: Pharmaceuticals
Leading Raw materials section and working in capacity of section head
? Assigning tasks and daily planning to subordinates ? New Vendors approval as an alternate source ? Updating status of all Sop’s & MOA according to current guidelines and pharmacopoeias ? Risk management of lab activities ? Responsible for “GLP” & “Safe lab practices” ? Authorized to provide First Aid in lab. ? To adhere monthly production schedule ? Approval of LIMS reports when required. ? Perform investigation related to OOS/OOT result and follow up root cause analysis as required and terminate it with CAPA. ? Handling of release activities in system.--
Officer quality control 09/2016 - 01/2021
Pharmevo pvt ltd, Karachi, sindh Pakistan
Industry: pharmaceutical
Has explored various functions of QC department as an analyst in Stablity studies Raw materials New product development Finish goods
Analysis for Raw Materials ? Standardization of Standards & maintain their Records ? Analysis of New Vendors Sample for New Molecule ? Documentation of Raw Material According to DRAP and Export Requirements. ? Analysis For Trial Batches ? Analysis For New Vendor Batches ? Preparation of Stability Protocols Log in incoming stability samples of commercial and new products in stability log books ? Maintaining intimation records of trail batches , pd batches , batches according to drap guideline. ? Analysis of nutraceutical products ? Monthly planning of Stability Products ? Maintain Inventory Record For Stability Products ? Maintain Records For Stability Chamber--

University of karachi 01/2011 - 12/2015
, , Pakistan
Degree: Bachelor's Degree
Major:Chemical engineering
? Heat & Mass Transfer ? Thermodynamics ? Chemical Reaction Engineering ? Risk Management & Environmental studies ? Fluid dynamics and Process Industries ? Maintenance & Gas engineering

Quailty control chemist, Laboratory, QMS, QHSE