Senior Specialist Regulatory Affairs

Abbott

Weesp, Netherlands
Not specified; not specified; local benefit pyckag...
Onsite
3-5 years regulatory affairs experience
Influenza vaccine regulatory strategies
Eu labeling and clinical module expertise
This role focuses on defining and maintaining regulatory strategies for influenza vaccines across developed and emerging markets

Job Summary

  • This role focuses on defining and maintaining regulatory strategies for influenza vaccines across developed and emerging markets.
  • The successful candidate will chair the Labeling SubTeam and serve as a key liaison for product lifecycle approvals including MAAs and renewals.
  • Abbott offers career development opportunities within an international company recognized as one of the most admired workplaces globally.

Matching Summary

This role focuses on defining and maintaining regulatory strategies for influenza vaccines across developed and emerging markets.

Salary

Not specified; Not specified; Local benefit package available

Skills & Requirements

Must-have

  • 3-5 years Regulatory Affairs experience
  • Influenza vaccine regulatory strategies
  • EU labeling and clinical module expertise
  • CCDS documentation maintenance
  • PSUR submission management

Nice-to-have

  • Dutch language proficiency
  • Curious and detail-oriented mindset
  • Collaborative cross-functional leadership
  • Proactive problem-solving under pressure

Key Requirements

  • Bachelor's or Master's degree in relevant field
  • Minimum 3-5 years in Regulatory Affairs
  • Strong knowledge of medicines registration requirements

Work Rights

Not specified

Tailored Resume

Cover Letter