About this Candidate
DAVRON CV: Candidate 1931169
BIOCHEMIST | ANALYTICAL SCIENTIST — HPLC, CE, METHOD DEVELOPMENT & QUALITY
Core Expertise
- Method development and validation for pharmaceutical analytical assays, including oncology therapies.
- HPLC and Capillary Electrophoresis expertise across PDA, UV, CAD, and fluorescence detection.
- Analytical techniques including Karl Fischer, DSC, NMR, GC, viscometry, and particle analysis.
- Quality and manufacturing support: batch documentation, SAP/Oracle tracking, and GMP-compliant operations.
- Scale-up support and pilot-plant correlation from benchtop trials to production processes.
Project Background
- Led method validation and feasibility trials supporting establishment of cancer therapy analytical methods.
- Executed routine and investigational assays with strict data integrity and detailed experimental documentation.
- Coordinated cross-functional teams to align production schedules, materials, and quality requirements.
- Developed analytical procedures enabling pilot-plant scale-up using benchtop correlations and small-batch trials.
- Maintained instrument calibration and performed troubleshooting across chromatography, spectroscopy, and rheology platforms.
Key Skills
- Chromatography: HPLC (PDA | UV | CAD | FLR) | GC | Capillary Electrophoresis | SEC
- Spectroscopy & thermal analysis: NMR | FTIR | UV-Vis | NIR | DSC
- Physical & particle analysis: Rheometry | Viscometry | Liquid Particle Analysis | Texturometry
- Specialized assays & tools: Karl Fischer | SoloVPE | Osmo | Peptide mapping | ADC free-drug testing
- Data systems & statistics: Empower 3 | LIMS | Oracle | SAP | ELN | Minitab | Microsoft Excel
- Quality & compliance: GMP | GDP | Aseptic techniques | 5S | Respirator training
Education
- MBA, Design Thinking and Innovation — John Brown University
- B.S., Biology (Genetics) — Pennsylvania State University
Why Interview this Candidate?
A laboratory-trained analytical scientist combining hands-on chromatography and biophysical assay expertise with an MBA perspective. Proven track record developing and validating analytical methods for high-value oncology therapies, supporting manufacturing and pilot-plant scale-up, and driving cross-functional quality compliance. Ready to contribute immediately to analytical, R&D, or quality teams.
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