Regulatory Affairs Associate

Ferring Pharmaceuticals

Turkey
Document lifecycle management
Regulatory submissions coordination
Local health authority interactions
The role involves serving as the Document Accountable Person and Controller to ensure document lifecycle management and compliance

Job Summary

  • The role involves serving as the Document Accountable Person and Controller to ensure document lifecycle management and compliance.
  • Candidates will coordinate new drug approvals, manage regulatory submissions, and support product lifecycle activities in line with local regulations.
  • Ferring offers an inclusive support package called Building Families at Ferring, providing equal policies for all employees regardless of location.

Matching Summary

The role involves serving as the Document Accountable Person and Controller to ensure document lifecycle management and compliance.

Skills & Requirements

Must-have

  • Document lifecycle management
  • Regulatory submissions coordination
  • Local health authority interactions
  • e-CTD and Veeva Vault experience
  • Artwork and labeling approval

Nice-to-have

  • Pricing data monitoring experience
  • Track Wise system knowledge
  • Eager to learn personality
  • Team player approach
  • Attention to details

Key Requirements

  • University degree in Pharmacy
  • 2-3 years practical experience in regulatory and quality assurance
  • Fluent English language skills

Work Rights

Not specified

Tailored Resume

Cover Letter