Strategic and result-driven M.Sc. Biotechnology graduate Professional with comprehensive knowledge of stability testing and regulatory requirements for medical devices/pharmaceuticals. Adept at leading 3 small technical projects from initiation to delivery, resulting in 25% improvement in project efficiency. Strong scientific background with expertise in analytical testing, technical writing, data analysis and quality compliance, contributing to 15% reduction in error rates. Excellent organizational skills to manage multiple priorities and meet deadlines with a 90% on-time project delivery record.
· Conducted routine laboratory testing for R&D projects involving techniques like HPLC, spectrophotometry, PCR, and electrophoresis.
· Prepared samples, solutions, and managed inventory of consumables for scheduled analysis per SOPs.
· Performed equipment maintenance, calibration and validated test methods ensuring data integrity.
· Documented experimental data with precision and organized records for reporting.
· Collaborated with teams to troubleshoot issues and ensure project milestones were achieved.
· Conducted routine QC testing of pharmaceutical products according to GLP and GMP protocols.
· Documented and reported test results, contributing to continuous improvement initiatives.
· Collaborated with production and development teams to resolve quality-related issues.
Stability Studies & Shelf-Life Testing - Technical Report Writing
Study Protocol Development - Regulatory Compliance (GMP, GLP)
Analytical Testing & Investigations - Project Management
Sample Management - Quality Actions & Change Control
Test Method Validation - Data Analysis & Documentation
ELISA - western blotting, SDS-Page, fluorescent immunoassays
Microscopy Training & Support
Image Analysis & Data Processing
Experimental Troubleshooting
Microsoft Office & Google Workspace
Critical Thinking & Continuous Learning
· Basic to Advance Excel
· Basic to Advance SQL