Toxikologe/Toxikologin

Slowenien

5 Jahre Erfahrung

Geburtsdatum:

Staatsangehörigkeit:
slowenisch

24719303

Hochschulstudium

Zeitraum
Abschluss / Fachbereich / Hochschule
Schwerpunkte

10/2008 – 09/2013

abgeschlossen

Doctor
Toxikologie
, Slowenien

Research of in vitro toxicology and carcinogenesis of HAA, which are known food carcinogens. I widen my knowledge in the fields of (genetic) toxicology and cell/molecular biology, covering a variety of laboratory practices and techniques used in above-mentioned fields. My research work was carried out in accordance with quality systems ISO 9001 and GLP that are established in laboratories of the Institute.

Berufserfahrung

Zeitraum
Tätigkeit / Unternehmen
Aufgaben

04/2014 – Bis heute

Pharmaceutical Inspector
, Slowenien

• inspection of good manufacturing and distribution practice of medicine manufacturers and distributors in Slovenia and abroad (e.g. India, China)

• writing SOPs and participation in the implementation of quality management system of the agency

10/2008 – 09/2013

Young Researcher
, Slowenien

• designing and performing the experiments in accordance with GLP standards
• performing toxicological tests
• evaluation of toxic and genotoxic effects of the compounds in accordance with OECD standards
• writing work reports and scientific articles
• presentation of results and participations at conferences
• mentoring and supervising the undergraduate students performing their research tasks
• participation in the implementation of quality management system
• management of laboratory supplies and relations with the suppliers

Sprachkenntnisse

Sprache
Level
Prüfung / Zertifikat
Slowenisch
Muttersprache

–

Englisch
Verhandlungssicher (C2)

–

Kroatisch
Konversationssicher (B2)

–

Deutsch
Grundkenntnisse (A1)

–

Weitere Fähigkeiten

Kompetenzen
Führerscheine
Interessen, Hobbys, Persönliches

Designing and performing the experiments in accordance with GLP standards.
Performing toxicological tests.
Evaluation of toxic and genotoxic effects of the compounds in accordance with OECD standards.
Writing work reports and scientific articles.

Working knowledge of ICH, PIC/S, Eudralex, WHO and some of the FDA guidelines for production, distribution and R&D for medicines and APIs.

QMS

  • PKW

So geht's