HIGHLIGHTS OF EXPERIENCE:
• Highly accomplished R&D Professional with experience in diverse areas encompassing Quality Audits, LC-MS/MS –small molecules , Quality Control Systems Implementation, Regulatory Compliance, Reporting & Documentation and General Management.
• Expertise and background on LC/MS-MS instrumentation, separation science and sample preparation techniques. Sound understanding of different aspects of in vitro/in vivo DMPK in drug discovery, development process and OECD-GCP/GLP regulatory guidelines. Knowledge in biology assays-Biomarker/LBAs & Phase I & II clinical trials.
• Proficiency in handling/review of complex projects like Novel drug delivery systems-Liposome’s/ C...