Abdul Taiyyab Bohra
Senior Analyst @Veeda Lifesciences
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WORK HISTORY
Senior Analyst @Veeda Lifesciences
Ahmedabad, IN
Performed bioanalytical sample analysis for pharmacokinetic (PK) and bioequivalence (BE) studies.Worked on LC-MS/MS / HPLC techniques for quantification of drugs and metabolites in biological matrices (plasma, serum, etc.).Conducted sample preparation techniques including protein precipitation, liquid-liquid extraction (LLE), and solid-phase extraction (SPE).Assisted in bioanalytical method development and validation as per regulatory guidelines (USFDA, ICH).Performed calibration curve preparation, QC sample analysis, and batch acceptance evaluation.Ensured compliance with GLP, cGMP, and data integrity (ALCOA+) principles.Handled chromatographic data processing and reporting using relevant software (add name if used, like Analyst/Sciex).Supported sample analysis for clinical trials and regulatory submissions.Participated in OOS/OOT investigations and documentation review.Maintained accurate laboratory records, logbooks, and audit-ready documentation.
EDUCATION
Gry Institute of Pharmacy Borawan
Bachelor of Pharmacy - BPharm
National Institute of Pharmaceutical Education and Research
MS Pharm in Biotechnology
ABOUT ABDUL TAIYYAB BOHRA
Welcome to my LinkedIn profile! I began my journey in the pharmaceutical world by earning a B Pharmacy degree from GRY institute of pharmacy borawan, where gained a solid foundation in pharmaceutical science Subsequently, I successfully cracked the prestigious national-level exams, GPAT(AIR 636) and NIPER JEE(AIR 1198), which the doors to one of the most esteemed institutions in the country - NIPER (National Institute of Pharmaceutical Education and Research).Here, I\'m Pursuing my post-graduation, I developed a strong foundation in biotechnology research and pharmaceutical sciences.I possess expertise in Biotechnology Research,pharmaceutical drug development, cell culture techniques, media preparation and bacterial culture techniques, production of biopharmaceutical, knowledge in regulatory guidelines and processes for pharmaceutical products, Project Management, which I am eager to apply to real-world challenges.Let\'s connect and explore synergies, share knowledge,and together contribute to the betterment of the pharmaceutical industry.\"
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