Anonymous | Explore Skills, Experience & Career Opportunities

Details

Skills

Analytical Method Transfer from R&D and sending units to QC
Pharmacopeial method validation (EP, BP, USP, JP)
Development and compilation of In-House Methods
Stability testing and raw material analysis under GMP
Risk assessment and audit trail review (21 CFR Part 11)
Nitrosamine analysis using LC-MS/MS and HS-GC/MS/MS
Instrument calibration, troubleshooting, and SOP creation
Stock management and procurement of lab consumables

About

Experienced and compliance-driven analytical forensic chemist with over 13 years of leadership in pharmaceutical quality control and forensic science. Currently serving as Head of QC Analytical Method Transfer at Remedica Pharmaceutical, I specialize in supervising method transfers, validating pharmacopeial methods, and managing raw material testing aligned with GMP, GLP, and international pharmacopeia standards (EP, BP, USP, JP). I lead a team of 15 analysts and oversee high-end instrumentation including LC-MS/MS, HS-GC/MS/MS, ICP-MS, and TOC analyzers.

My career began in forensic toxicology at the State General Laboratory of Cyprus, where I conducted criminal casework and collaborated with international agencies including ENFSI, UNODC, and BKA Wiesbaden. I hold an MSc in Forensic Science from the University of Strathclyde and a BSc (Hons) in Forensic Science from the University of Derby, with published research in gunshot residue and psychotropic drug detection.

I bring a rigorous, documentation-focused approach to method development, audit readiness, and regulatory compliance, with proven expertise in analytical risk assessment, audit trail review (21 CFR Part 11), and nitrosamine analysis. Fluent in English and Greek, I am a member of multiple professional bodies including the Forensic Science Society and the Pancyprian Union of Chemists.