Director, Regulatory Affairs Operations & Publishing (pharma)

Alcon

Fort Worth, TX, US
Onsite
10 years of relevant experience
6 years of demonstrated leadership
Veeva rim suite proficiency
This role is part of Alcon's Quality & Regulatory Affairs function, ensuring products meet global and local regulations

Job Summary

  • This role is part of Alcon's Quality & Regulatory Affairs function, ensuring products meet global and local regulations.
  • The Director will lead teams in dossier preparation, submission management, and maintaining the Veeva RIM Suite.
  • Alcon offers a robust benefits package including health, life, retirement, and flexible time off for exempt associates.

Matching Summary

This role is part of Alcon's Quality & Regulatory Affairs function, ensuring products meet global and local regulations.

Skills & Requirements

Must-have

  • 10 years of relevant experience
  • 6 years of demonstrated leadership
  • Veeva RIM Suite proficiency
  • GxP regulatory compliance
  • Dossier preparation and publishing

Nice-to-have

  • Strategic product direction skills
  • Continuous improvement initiatives
  • Cross-functional team collaboration
  • Inclusive culture mindset
  • Global eye health passion

Key Requirements

  • Bachelor's Degree or equivalent experience
  • 10 years of relevant experience required
  • 6 years of demonstrated leadership experience
  • Fluent English communication skills
  • Onsite work in Fort Worth, TX

Work Rights

Not specified

Tailored Resume

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