Regulatory Affairs And Pharmacovigilance Specialist

ferring.in

London, United Kingdom
Hybrid
Minimum 3 years regulatory experience
Knowledge of uk regulatory environment
Post-brexit regulatory requirements knowledge
The role involves preparing, reviewing, and submitting variations, renewals, and new product authorizations while maintaining the local UK Pharmacovigilance System Master File

Job Summary

  • The role involves preparing, reviewing, and submitting variations, renewals, and new product authorizations while maintaining the local UK Pharmacovigilance System Master File.
  • Ferring Pharmaceuticals offers an empowering, entrepreneurial culture focused on scientific advances in reproductive health, gastroenterology, and urology.
  • Employees are expected to live within a reasonable commutable distance due to a hybrid working arrangement requiring a minimum of three days in the office weekly.

Matching Summary

The role involves preparing, reviewing, and submitting variations, renewals, and new product authorizations while maintaining the local UK Pharmacovigilance System Master File.

Skills & Requirements

Must-have

  • Minimum 3 years Regulatory experience
  • Knowledge of UK Regulatory environment
  • Post-Brexit regulatory requirements knowledge

Nice-to-have

  • Direct MHRA communication experience
  • UK Pharmacovigilance work experience
  • Entrepreneurial spirit and curiosity

Key Requirements

  • Life Science degree or equivalent
  • Minimum 3 years pharmaceutical regulatory experience
  • Mandatory knowledge of UK post-Brexit regulations

Work Rights

Not specified

Tailored Resume

Cover Letter