Offer summary
Qualifications:
Bachelor’s degree plus 8 years in Regulatory Operations, Expertise in eCTD dossier management preferred, Experience with global regulatory submission processes, Advanced MS Suite and Smartsheets user, Experience with Veeva RIM systems is a plus.
Key responsabilities:
- Oversee all regulatory submissions and compliance
- Manage publishing of submissions to health authorities
- Develop and maintain regulatory standards
- Evaluate and improve regulatory systems
- Lead regulatory project management activities