
Regulatory Affairs Lead Specialist
1 day ago
About the Role
We are seeking a highly skilled Regulatory Affairs Senior Officer to lead the preparation and management of regulatory dossiers, ensuring compliance with regulations and supporting the approval and registration of our pharmaceutical products.
Key Responsibilities- Develop and maintain in-depth knowledge of global regulatory guidelines and requirements.
- Organize and manage complex documentation, including CTD and ACTD dossiers, COPP, and FSC, with exceptional attention to detail and precision.
- Collaborate with cross-functional teams to ensure seamless communication and efficient project execution.
- Utilize effective time management skills to meet critical deadlines and drive projects forward.
This is an excellent chance to join our organization and contribute to the development and commercialization of innovative pharmaceutical products.
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