Designing, fabricating, and optimizing inorganic perovskite solar cell devices and thin-films, executing research projects in a timely and systematic manner.
Thin Films Coatings and Deposition using Spin-Coating and Glove box vacuum Evaporator (PVD).
Designed and executed thin films characterization using UV-Vis spectroscopy, photoluminescence, SEM, XRD, XPS, and JV to evaluate structure-performance relationships.
Applied the scientific method to test hypotheses related to material composition, processing conditions, and performance outcomes, resulting in data-driven conclusions and clear recommendations for performance improvements.
Led material optimization efforts by modifying chemical formulations and processing parameters to improve efficiency, durability, and reproducibility-similar to product redesign and performance enhancement initiatives.
Documented novel material strategies and process improvements to support proprietary research development.
Performed statistical data analysis using Excel and Origin Pro software to interpret experimental results and guide decision-making.
Scientific writing, including my master's thesis and a paper to publish in a peer-reviewed journal.
Researcher
Nankai University
Tianjin
08.2018 - 03.2020
Designing and fabricating nucleic acid based Bioassays to analyze and detect small biological molecules including DNA and RNA for diagnosis.
PCR-based assays for detection of microRNA.
Used fluorescence dyes and fluorescence measurements for detection.
Worked on Gel Electrophoresis, cell culture, and real-time fluorescence spectrometry.
Quality Control Chemist
Solaris Life Sciences
Rawalpindi
12.2019 - 12.2021
Hands-on experience using GC and LC-MS techniques to analyze and detect drug-related molecules.
Aid in the formulation of drugs, rational design for active ingredients concentration, and choice of solvents and stabilizers to improve efficacy and shelf life.
Worked in compliance with Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to ensure the quality of finished products as well as the safety of personnel.
Performed routine chemical testing of raw materials, in-process samples, and finished products.
Stability measurements of finished products using trend analysis by tracking pH, degradation products, and dissolution.
Followed compendial methods in accordance with USP (United States Pharmacopeia), EP (European Pharmacopoeia).
Calibrated and maintained analytical instruments, including HPLC, GC, pH meters, analytical balances, and Karl Fischer titrator to ensure accuracy and reliability of results.