Senior Regulatory Affairs Specialist

Kenvue

Reading, Berkshire, United Kingdom
Hybrid
Eu regulatory requirements and guidelines
Mrp or dcp submission experience
Health authority communication skills
The role is accountable for all regulatory activities associated with EMEA medicinal products including new submissions and variations

Job Summary

  • The role is accountable for all regulatory activities associated with EMEA medicinal products including new submissions and variations.
  • Kenvue is a global team of approximately 22,000 people passionate about insights, innovation, and delivering the best products to customers.
  • The position offers a competitive benefit package including paid holidays, volunteer time, summer Fridays, and learning opportunities.

Matching Summary

The role is accountable for all regulatory activities associated with EMEA medicinal products including new submissions and variations.

Skills & Requirements

Must-have

  • EU regulatory requirements and guidelines
  • MRP or DCP submission experience
  • Health Authority communication skills
  • Project prioritization and timeline management
  • Audit preparation and inspection support

Nice-to-have

  • Consumer healthcare environment knowledge
  • Process improvement initiative ownership
  • Multi-cultural matrix organization collaboration
  • Crisis management and sensitive issue handling

Key Requirements

  • Bachelor's Degree or higher
  • 4+ years related regulatory experience
  • Experience on non-prescription EU procedures (MRP/DCP)
  • Proficiency in English

Work Rights

Not specified

Tailored Resume

Cover Letter