Offer summary
Qualifications:
University-level education in Life Sciences or equivalent experience, Extensive regulatory affairs experience in pharmaceuticals, Strong understanding of CMC and post-approval regulations, Experience in writing CMC regulatory documents, Fluent in English, proficiency in Office tools.
Key responsabilities:
- Lead projects ensuring successful planning and execution
- Act as primary client contact for project communications
- Develop submission strategies for CMC activities
- Coordinate submissions with various departments
- Mentor junior team members and identify new business opportunities