Labelling and Compliance Manager
Há 7 dias
We are looking for a talented Regulator Affairs Expert - Labelling to join our team at TN Portugal. In this role, you will be responsible for planning and expediting approval projects using software tools, including databases and document management systems.
You will work closely with internal/external stakeholders to ensure effective communication and coordination of project teams. A strong understanding of ICH regions and EU regulations is required.
This is an exciting opportunity to join a dynamic team and contribute to delivering high-quality regulatory submissions and labelling activities.
- Main Responsibilities:
- Plan and expedite approval projects using software tools
- Closely monitor and adhere to timelines
- Communicate effectively with internal/external stakeholders
Requirements:
- Education: Bachelor's degree in pharmacy, medicine or other life sciences, or a bachelor's degree in science, engineering, or mathematical domain
- Experience: Professional experience in regulatory affairs with a profound track record in labeling activities for innovator drugs on a global level
- Skills: Proficiency in databases, labeling software tools, and project management software
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