Research Scientist

  • by
Location
Candidate No.
1886843

About this Candidate

DAVRON CV: Candidate 1886843

SENIOR ANALYTICAL SCIENTIST | QUALITY SYSTEMS, METHOD DEVELOPMENT & ISO AUDITING

Core Expertise

  • Leading quality investigations, root cause analysis, CAPA and deviation management under cGMP and ISO frameworks.
  • Developing and transferring analytical methods (HPLC, LC‑MS, GC) with USP/EP compendial compliance.
  • Managing laboratories, supervising scientific and non-scientific staff, and ensuring regulatory readiness.
  • Performing environmental and effluent testing aligned with EPA and environmental reporting guidelines.
  • ISO 9001 Lead Auditor and ISO 17025 experience driving quality management system improvements.

Project Background

  • Validated SOPs and batch production records to meet GLP/GMP compliance across R&D and manufacturing.
  • Led method development projects for APIs, fine chemicals, and lipid-related compounds with scale-up.
  • Executed analytical transfers and technology handovers between labs, vendors, and pilot facilities.
  • Conducted root cause investigations for OOS/OOT events, reducing recurrence through targeted CAPA actions.
  • Implemented KPIs and audit programs to monitor quality performance and ISO regulatory adherence.

Key Skills

  • HPLC | UPLC | GC | GC‑MS | LC‑MS | QTOF | Mass spectrometry | FTIR | NMR
  • Method development & validation | USP | EP | JP compendial protocols
  • Quality systems: ISO 9001 | ISO 17025 | cGMP | GLP | FDA 21 CFR
  • Lab informatics: LIMS | SAP | QT9 | Empower | ChemStation | OpenLab
  • Investigations: RCA | OOS/OOT | CAPA | Deviations | Risk assessments
  • SOP & BPR authoring, document control, and validation transfers

Education

  • Post-Doctoral Fellow — University of Florida
  • Ph.D., Chemistry — CDRI / BR Ambedkar University
  • PGDM, Business Management — Bhavan Institute

Awards & Recognition

  • Four patents and 20+ peer-reviewed publications and conference presentations
  • Zero-Harm Lead recognition for safety leadership (2022–2023)
  • Multiple consecutive 'Outstanding Accomplishment' awards in drug discovery research

Why Interview this Candidate?

They combine a PhD and a decade of industrial analytical experience with proven success in method development, ISO auditing, and lab leadership. Holder of multiple patents and extensive instrumentation expertise, they consistently drive regulatory-compliant quality improvements and technology transfers that reduce risk and improve operational performance.

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