Sr. Regulatory Affairs manager

The purpose of this mail is to discuss the below job opportunity, that can be a great fit for you.

About Organization: Novo Medi Science

Vacancy Details:

Regulatory Expertise: Manage the regulatory process for Pharmaceutical Finished Formulations across CIS, LATAM, and Africa.

Dossier Management: Compile and review ACTD and CTD dossiers to ensure accuracy and compliance.

Compliance: Review product artworks and samples to ensure compliance with regulatory requirements.

International Coordination: Liaise with international agents for dossier submission, follow-up, and product registration.

Documentation: Maintain comprehensive records of technical documentation, product registrations, and related expenses.

Experience in compiling and reviewing ACTD and CTD dossiers.

Proficiency in handling MOH queries and ensuring timely responses.