• Manage ADR (adverse drug reaction) forms and other regulatory data.• Authored SOP.• Proceed under SOP and maintain regulatory compliance.• Good knowledge of different spectroscopy, chromatography, and other laboratory devices like pH meters.• able to do CADD (Computer-Aided Drug Design) with different applications and also work on SnapGene Viewer and PyMol.• Developed schedules in Microsoft Project.• Excellent verbal and written communication skills.• Ability to resolve conflicts during work and sharp critical thinker.• Potential to pay the required attention to details, documentation, and equipment maintenance.• Perform required multiple tasks at the same time.• Good in safe specimen handling, data and statical analysis, quality control guidelines, and medical research.• Certified Worker health and safety Awareness Program by OHSA and WHMIS.