Akash Kadam

Background

About Akash Kadam

I am a dedicated life-science professional with a Master’s in Pharmaceutical Business and Technology (Level 9 QQI) from Innopharma, Griffith College, and a Bachelor’s in Pharmacy. With hands-on experience in laboratory testing, quality control, and documentation aligned with GMP and ALCOA+ principles. Skilled in analytical techniques including HPLC, UV-Vis, and wet chemistry, with hands-on experience in reagent preparation, equipment calibration, and sample analysis. Passionate about ensuring product quality, regulatory compliance, and continuous improvement within pharmaceutical and biotech environments. As a Pharmacovigilance Junior Data Analyst at Cognizant, I managed regulatory submissions for AbbVie products (Humira, Imbruvica, Skyrizi), ensuring compliance with MedDRA and WHO standards. My work involved preparing MedWatch and CIOMS reports with 99% accuracy, handling over 2500 patient reports, and collaborating closely with regulatory teams to support global product registrations. Currently seeking opportunities in Quality Control and Environmental monitoring, where I can contribute my laboratory knowledge, regulatory awareness, and analytical skills to support high-quality pharmaceutical outcomes. Core Skills- HPLC - UV-Vis Spectrophotometry - Quality Control - Good Manufacturing Practice (GMP)- Good Laboratory Practice (GLP)- ALCOA+ Principles - Analytical Testing - Documentation and Data Integrity - Regulatory Compliance - SOPs and Validation - Dissolution Testing - Calibration - QA/QC - Pharmaceutical Manufacturing - Regulatory submissions (FDA, EMA)- Electronic document management (Microsoft Office, Adobe Acrobat, VEEVA)- Lean Six Sigma for process improvement - Cross-functional collaboration Certifications: Advanced Certificate in Clinical Research Pharmaceutical & Medical Device Innovations (Univ. of Minnesota) Project Management (PMP training)