Senior Regulatory Affairs Specialist

Bristol Myers Squibb

Australia
**
3 years prescription medicine experience
Knowledge of australia/new zealand regulatory processes
Tertiary qualification in medicine pharmacy or life science
** Bristol Myers Squibb is seeking a Senior Regulatory Affairs Specialist in Australia to manage regulatory activities for assigned products, ensuring compliance and timely product variations. The role requires a strong understanding of regulatory processes and collaboration with internal and external stakeholders. **

Job Summary

  • The role involves planning and executing timely product variations and ensuring regulatory compliance for BMS products supplied in Australia and New Zealand.
  • Employees will manage interactions with Health Authorities, track changes in regulatory requirements, and communicate regulatory intelligence effectively to various stakeholders.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs designed to support employees in pursuing their goals both at work and in their personal lives.

Matching Summary

Match Score: 75

** Bristol Myers Squibb is seeking a Senior Regulatory Affairs Specialist in Australia to manage regulatory activities for assigned products, ensuring compliance and timely product variations. The role requires a strong understanding of regulatory processes and collaboration with internal and external stakeholders. **

Skills & Requirements

Must-have

  • 3 years prescription medicine experience
  • Knowledge of Australia/New Zealand regulatory processes
  • Tertiary qualification in medicine pharmacy or life science

Nice-to-have

  • Post graduate qualifications well regarded
  • Ability to negotiate with diverse teams
  • Experience with Medicines Australia working groups

Key Requirements

  • Degree in medicine, pharmacy, or life science
  • Minimum 3 years relevant prescription medicine experience
  • Working knowledge of drug development process from discovery to marketing

Work Rights

Not specified

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