This document contains the resume of Hassan Haider Siddiqui. It includes his personal details like name, date of birth, address and contact information. It outlines his objective of pursuing a challenging career. His professional experience includes current and previous roles in quality control and R&D at pharmaceutical companies. Responsibilities included supervising validation studies, analytical method development and testing. The document also lists his educational qualifications and certifications obtained, as well as achievements and personal skills.

1. Hassan Haider Siddiqui Cell # : 0336-2016809, 0325-2121171
Email : hassaan.haider@yahoo.com
Address : R-75 Rehman Villas Scheme 33 UC 12
Main University Road Karachi Pakistan.
PERSONAL Full Name : Hassan Haider Siddiqui
Father’s Name : Jamal Haider Siddiqui
Date Of Birth : August , 1, 1989
Place Of Birth : Islamabad
NIC # : 42201-2855848-3
OBJECTIVE Looking forward to pursue a challenging career & having the opportunity
to work in an innovative and efficient standard by offering my full
dedication and commitment.
EMPLOYEMENT Assistant Manager Quality Control
SAMI Pharmaceuticals Pvt Ltd
August-2022 – To date
Major Responsibilities :
 To Supervise Process Validation and Analytical Method Validation
teams for smooth testing and reporting of process validation samples
and validation of analytical methods to shift from non-pharmacopeia
methods to pharmacopeia and Optimization of methods to lab
environment.
 To Supervise Trial & Development Batches Testing and Analytical
Method Development to shift from non-pharmacopeia methods to
pharmacopeia and Optimization of methods to lab environment.
 To Supervise Comparative Dissolution Profile and Pharmaceutical
Equivalence Studies between RLD and test product to evaluate
similarity for BE purpose and for product dossier in regulated markets
and local product launch DRAP.
 To Supervise Compliance against ISO/WHO and PIC’s guidelines for
Data Integrity, Data Traceability, Qualification and Calibration of Lab
and Laboratory equipment’s.
 To Perform Cleaning Validation to evaluate effective cleaning
procedure and reduce risk of cross contaminations.
 To Perform Dose Solubility Studies and Solution Stability to evaluate
sink conditions and degradation.
 Standardization of working standards against Pharmacopeia and
Manufacturers Reference Standards.
 Calibration/Performance Qualification of Lab Instruments: pH Meter,
Conductivity Meter, Electronic Weight balance, Dissolution
Apparatus, HPLC.
 Training on Different SOPs, QMS System, Guidelines and different
studies to team.

2. Assistant Manager R&D-AL
Getz Pharma Pvt Ltd
January-2019 –July-2022
Major Responsibilities :
 To Supervise Raw Material Testing of API to evaluate its Physical and
Chemical properties and Vendor Management through Change Alert
and Risk Assessment.
 To Supervise Analytical Method Development to shift from non-
pharmacopeia methods to pharmacopeia and Optimization of
methods to lab environment.
 To Supervise Comparative Dissolution Profile and Pharmaceutical
Equivalence Studies between RLD and test product to evaluate
similarity for BE purpose and for product dossier in regulated markets
and local product launch DRAP.
 To Perform/Supervise Validation/Verification of API and Finished
Product for method Linearity, Repeatability, Accuracy, Robustness
and to establish LOD and LOQ Levels.
 To Perform Stability of Finished Product on several intervals for both
accelerated and RT to interpolate shelf life of product and to evaluate
product safety and efficacy throughout its shelf life.
 To Perform Particle Size Analysis and limit establishment of particle
size.
 To Perform Dose Solubility Studies and Solution Stability to evaluate
sink conditions and degradation.
 Standardization of working standards against Pharmacopeia and
Manufacturers Reference Standards.
 Calibration/Performance Qualification of Lab Instruments: pH Meter,
Conductivity Meter, Electronic Weight balance, Dissolution
Apparatus, HPLC.
 Training on Different SOPs, QMS System, Guidelines and different
studies to team.
Sr. Executive-R&D-AL
Getz Pharma Pvt Ltd
January-2017 – December-2018
Major Responsibilities :
 To Perform Comparative Dissolution Profile/Pharmaceutical
Equivalence Studies of Test Product against Innovator.
 To Perform Stability Studies of finished product.
 To Perform Raw Material Testing and Verification/Validation of raw
material.
 To Perform Verification/Validation of finished product.
 To Perform Particle Size Analysis.
 Standardization of Working Standards against Pharmacopeia
Reference Standards.
 Calibration of Lab Instruments:
pH Meter, Conductivity Meter, Analytical/Semi-Micro & Micro
weighing balances ,Dissolution Apparatus ,HPLC

3. Executive-R&D-AL
Getz Pharma Pvt Ltd
September 2015 – December-2016
Major Responsibilities :
 To Perform Comparative Dissolution Profile/Pharmaceutical
Equivalence Studies of Test Product against Innovator.
 To Perform Raw Material Testing and Verification/Validation of raw
material.
 To Perform Trial & Development testing of finished products.
 To Perform Particle Size Analysis of raw materials.
 Standardization of Working Standards against Pharmacopeia
Reference Standards
QC-Chemist
Tufail Chemical Industries
August 2014 – September 2015
Major Responsibilities :
 Preparation and Standardization of Standard Solutions
 Calibration of Lab Instruments like: pH Meter, TDS Meter, Lovibond
Tintometer, Electronic Weight balance.
 Raw Material Testing.
 In-Process Testing.
 Product Testing.
EDUCATION
CERTIFICATIONS
ACHIEVMENTS
MSc Applied Chemistry & Chemical Technology
University Of Karachi
June 2015
BSc Hons Applied Chemistry & Chemical Technology
University Of Karachi
June 2014
Intermediate Pre Engineering
Govt. Degree College Stadium Road Karachi
June 2009
Matric Science Group
Green Land Public School Karachi
June 2006
 Lean Six Sigma Yellow Belt from PIQC (Dec-2022).
 Awareness and Internal Audit ISO/IEC 17025 from HSEQ (Jan-2023)
 Participated 3 times in successful Product Development with CDO, 2
times in WHO Prequalification of Organization, through comparative
testing of innovator/CDO/Test product.
 Participated in PIC’s Prequalification of Organization, through
producing good quality documents of comparative testing of
innovator and Test product for dossier submission.

4. PERSONAL SKILLS
 Critical Thinking.
 Team work.
 Leadership.
 Flexibility.
 Vendor Management.
REFRENCE Reference will be furnished upon request.