Regulatory Affairs Analyst

Alcon

Warsaw, Poland
Attractive base salary; annual bonus; attractive b...
Hybrid
2 years experience in regulatory affairs function
University degree in life sciences or pharmacy
Veeva rim system knowledge for submissions
This role supports the Regulatory Affairs EMEA team by coordinating administrative activities, managing suppliers, and handling Veeva RIM submission processes

Job Summary

  • This role supports the Regulatory Affairs EMEA team by coordinating administrative activities, managing suppliers, and handling Veeva RIM submission processes.
  • Candidates will be responsible for maintaining regulatory databases, generating KPI reports, and executing sample requests for registration in EMEA markets.
  • The position offers a hybrid work model, flexible hours, and an opportunity to work in a best-in-class medical device organization with a global team.

Matching Summary

This role supports the Regulatory Affairs EMEA team by coordinating administrative activities, managing suppliers, and handling Veeva RIM submission processes.

Salary

Attractive base salary; Annual bonus; Attractive benefits package

Skills & Requirements

Must-have

  • 2 years experience in Regulatory Affairs function
  • University degree in Life Sciences or Pharmacy
  • Veeva RIM system knowledge for submissions

Nice-to-have

  • Action-oriented mindset with sense of urgency
  • Strong communication and collaboration skills
  • Experience managing multiple tasks in agile environment

Key Requirements

  • 2 years RA function experience
  • University degree in Biology, Chemistry, Pharmacy, or Law
  • Fluent English spoken and written

Work Rights

Not specified

Tailored Resume

Cover Letter