Gain hands-on experience in pharmaceutical regulatory processes while supporting critical documentation and compliance activities
Job Summary
Gain hands-on experience in pharmaceutical regulatory processes while supporting critical documentation and compliance activities.
Develop your regulatory knowledge by studying Czech and European legislation, including Identification of Medicinal Products (IDMP) requirements and relevant guidelines.
Enjoy flexible part-time hours (80 hours/month) designed to complement your studies while providing meaningful professional experience.
Matching Summary
Gain hands-on experience in pharmaceutical regulatory processes while supporting critical documentation and compliance activities.
Skills & Requirements
Must-have
Vault RIM system
Regulatory documentation
English and Czech language proficiency
MS Office applications
Nice-to-have
Pharmaceutical industry experience
Engaged and proactive attitude
Systematic approach to work
Key Requirements
Currently enrolled student in Medicine, Pharmacy, Public Health, Biology, or Chemistry