Intern- Regulatory Affairs

539

Singapore, Singapore
Hybrid
Apac region submissions
New product registrations
Life-cycle submissions
Our company starts your journey on the career path within the pharmaceutical industry

Job Summary

  • Our company starts your journey on the career path within the pharmaceutical industry.
  • The Intern will be involved in and responsible for the execution and management of the APAC region submissions including new product registrations and life-cycle submissions to keep our products compliant and available for patients.
  • This internship will be completed in a hybrid model (virtual and/or on-site).

Matching Summary

Our company starts your journey on the career path within the pharmaceutical industry.

Skills & Requirements

Must-have

  • APAC region submissions
  • new product registrations
  • life-cycle submissions
  • assess changes to dossiers
  • liaise with colleagues globally
  • review submission packages

Nice-to-have

  • operational excellence projects
  • developing best practises
  • learn regulatory policy
  • advocacy
  • intellectually curious
  • healthy debate

Key Requirements

  • Diploma or BSc in a scientific discipline
  • third or penultimate year of study
  • 6-month placement
  • analytical skills
  • detail-oriented

Work Rights

Not specified

Tailored Resume

Cover Letter