Artem Akhtiamov - Резюме Quality assurance , Pharmacovigilance, Production worker, Warehouse worker

Pharmacist Mar 2025 — Jan 2026 Vitta· Moscow, Russia — Reviewed and validated prescriptions for accuracy, completeness and clinical appropriateness, escalat- ing discrepancies to prescribers where required. — Advised patients on correct medication use, dosing, adverse effects and drug–drug interactions, sup- porting treatment adherence and patient safety. — Maintained documentation and product handling in line with national pharmaceutical regulations and storage requirements. Laboratory Assistant Aug 2025 — Oct 2025 Institute of Parasitology· Moscow, Russia — Performed gel electrophoresis, DNA extraction and quantitative spectrophotometric determination of bacterial DNA. — Prepared samples for High-Performance Liquid Chromatography (HPLC) and interpreted resulting chro- matograms. — Documented experimental procedures and results according to laboratory protocols and good docu- mentation practice. Scientific Writer & Research Contributor Jul 2025 — Nov 2025 Academic projects — Co-authored and edited a literature review, The Use of Monoclonal Antibodies for the Therapy of Rheumatoid Arthritis, prepared for submission to Bentham Science. — Authored a full research thesis, The Role of the BDNF System in the Pathogenesis and Therapeutic Strategy of Generalized Anxiety Disorder, covering literature appraisal, data interpretation and scien- tific argumentation in English

Specialist Degree in Pharmacy (MPharm equivalent, 300 ECTS) Sechenov University — First Moscow State Medical University Graduated with Distinction (Diploma with Honours). Qualification: Pharmacist (Provizor), speciality 33.05.01 Pharmacy. Full-time, 5 years.

Analytical | HPLC sample preparation and chromatogram interpretation, gel electrophoresis, UV/Vis spectrophotometry, DNA extraction Pharmaceutical | Pharmaceutical care, drug interaction analysis, pharmacotherapy, pharmaceutical tech- nology, pharmacognosy, toxicological chemistry Regulatory & Quality | Pharmaceutical legislation, good practices in the circulation of medicinal prod- ucts (GxP fundamentals), quality control of medicines Documentation | Scientific and medical writing, literature review, academic translation of scientific texts, MS Office (Word, Excel, PowerPoint) Personal | Attention to detail, structured documentation discipline, adaptability, cross-cultural commu- nication

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Russian — Native
English — Fluent — C1
Serbian — Elementary — A2, in progress