About this Candidate
DAVRON CV: Candidate 3812251
PROCESS ENGINEER | PHARMACEUTICAL MANUFACTURING | COMMISSIONING, VALIDATION & AUTOMATION
Core Expertise
- Process optimization and continuous improvement within regulated pharmaceutical manufacturing environments.
- Equipment commissioning, IQ/OQ/PQ documentation, and qualification of clean utilities and production lines.
- Automation design and implementation using Allen-Bradley PLCs, HMI interfaces, and SCADA monitoring.
- Risk assessment and safety improvement via HAZOP, root-cause analysis, and Lean Six Sigma methods.
- Pharmaceutical laboratory techniques, dissolution studies, HPLC, UV-Visible analysis, and CFD-based hydrodynamics.
Project Background
- Supported greenfield commissioning of aseptic cleanrooms, lyophilizers, filling lines, and purified-water systems.
- Led equipment evaluation and procurement coordination using AutoCAD and SolidWorks, delivering ~$100,000 reported savings.
- Conducted HAZOPs and safety reviews that contributed to a reported 30% reduction in process incidents.
- Implemented SCADA-based monitoring of critical parameters, contributing to a reported 15% reduction in production time.
- Prepared and maintained over 100 validation reports, SOPs, and compliance documents for regulated manufacturing.
Key Skills
- AutoCAD | SolidWorks | Aspen HYSYS | Python | Microsoft Excel
- SCADA systems | Allen-Bradley PLCs | HMI interfaces
- CFD | HPLC | UV-Visible spectrophotometry | Dissolution testing
- Process validation | IQ/OQ/PQ | SOP development | GMP compliance
- HAZOP | Root-cause analysis | Lean Six Sigma | Continuous improvement
Education
- M.S., Chemical Engineering — New Jersey Institute of Technology
Why Interview this Candidate?
A process engineer with a master's degree and hands-on experience in regulated pharmaceutical manufacturing. Delivered measurable results—including ~$100k in project savings, a reported 30% reduction in incidents, and a 15% production time improvement—through commissioning, automation, and process optimization. Brings strong validation documentation experience, PLC/SCADA automation skills, and proven HAZOP and continuous-improvement capabilities to accelerate reliability and compliance.
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