PRABHJOT KAUR

Competent in analyzing pharmaceutical raw material and finished product for chemical and microbiological parameters using analytical instrumentations and connected software, wet chemical analysis, and sterility techniques. Expertise in good documentation of data collected and following Good Laboratory Practices (GLP), and Standard Operating Procedure (SOP) to maintain safety and quality in lab environment. HIGHLIGHTS OF QUALIFICATIONS: Pursued University Degree in Biotechnology and completed College Diploma in Advance Biotechnology. Performed instrumental analysis of pharmaceutical materials and acquired data from instrument software by implementing knowledge gained while analyzing materials in college instrumental laboratory. Followed various pharmacopeias (USP, BP, and IP) to perform analysis of pharmaceutical materials in previous organizations and in college pharmaceutics laboratory. Acquired Good Laboratory Grades in analytical chemistry lab in college. Acquired good grades in accuracy and precision in various analysis done in college’s analytical chemistry and analytical instrumentation lab. Worked in a team and individually to complete analysis of a given material in previous organization and in college. Completed various testing parameters simultaneously while managing time efficiently without affecting the quality of results. Demonstrated proficiency in Microsoft Excel and Word to produce effective data documentation and record keeping. Performing SDS-PAGE, Chromatography techniques: Ion chromatography, size column Chromatography, Gas Chromatography, Blotting techniques, Polymerase chain reaction, Transcription, and translation of gene. Knowledge of techniques in a biochemistry / biotechnology discipline, e.g. protein expression/purification, HPLC , SDS-PAGE/western blot, electrophoresis, CE, enzyme assays, ELISA, PCR, DNA isolation, restriction enzyme digestions, cell culture, bacteria culture. Perform analyses using HPLC, UPLC, GC, UV, FTIR, and numerous other analytical methodologies and techniques. Performed laboratory analysis on drug substances and products, conducting investigations on out-of-specification (OOS) and out-of-trend (OOT) results, as well as instrument-related issues. Ensured compliance with company SOPs, regulatory requirements, and safety standards. Conducted calibration and qualification programs for laboratory equipment, adhering to guidelines and procedures to ensure accurate measurements and reliable results.

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