Summary

Qualitative and quantitative testing of raw materials and finish products by using UV/VIS spectrophotometer, HPLC, by titration as per SOP and pharmacopoeia guideline.
Prepare the certificate of analysis for raw materials and finished products.
Perform in-process quality assurance checks for tablets, capsules, and liquid orals.
Preparation of standard operating procedure (SOPs) of raw material and finished products.
Good in instrument handling like TOC, Muffle furnace, Melting point apparatus, UV/VIS spectrophotometer, and Dissolution apparatus.
Testing of packaging material as per SOPs.

Experience

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Senior Analytical Method Validation Analyst
Remington Pharmaceutical Industry
Dec 2021 - Present | Lahore, Pakistan

Perform analytical method validationPerforming cleaning validationPerforming process validationTesting of stability studies of existing productsChange controlDeviationRisk assessment

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Officer QA lab operation
Remington pharmaceutical industry
Feb 2021 - Dec 2021 | Lahore, Pakistan


Key responsibilities:
Verify the testing in quality control lab. 
Review the documents of quality control lab. 
Sample tracking and receiving. 
Review the audit trail of instruments

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QC analyst
Revive Pharmakon
Jan 2019 - Jan 2021 | Lahore, Pakistan



Education

University of Lahore
Masters, MSc, ‎
Chemistry
CGPA 3.8/4
2018

Skills

Intermediate Analytical Skills
Expert Auditing
Intermediate Chemical Formulation
Expert Data Quality Control
Beginner Extrovert
Intermediate Fluent in English
Intermediate Interpersonal Leadership
Intermediate Laboratory Quality Assurance
Intermediate Legal Documents Management
Intermediate Quality Control Processes Command
Expert Reasrch and Development
Expert Resourceful Problemsolving
Expert Written Oral and Communication
Intermediate إعلانات المبيعات

Languages

Expert Punjabi
Expert Urdu
Intermediate English