A company is looking for a Senior Regulatory Affairs Specialist - Pharma (Remote).
Key Responsibilities :
Oversee end-to-end dossier execution activities including submission planning and execution throughout a product's lifecycle
Collaborate with Regulatory Leads and cross-functional content authors to develop and maintain submission content plans
Provide input and guidance on submission processes, compliance, and deliverables as a Regulatory Operations representative
Required Qualifications :
Bachelor's degree or equivalent work experience
7+ years of Regulatory Operations experience in pharmaceutical drug development and global submissions
3+ years of eCTD publishing experience
Demonstrated expertise with eDMS applications and publishing systems
Knowledge of 21 CFR Part 11 compliance and software / system validation
Regulatory Specialist • Des Moines, Iowa, United States