Senior Regulatory Submissions Lead - Hybrid

AbbVie, a global biopharmaceutical company, seeks a Senior Associate Regulatory Affairs Submission Management for a hybrid schedule in Florham Park, NJ. You will manage medium to high impact regulatory submissions, coordinate publishing activities, and partner with cross‐functional teams to ensure timely, compliant dossiers. The role requires 4+ years in regulatory affairs or related fields with publishing software proficiency; PMP and RAC credentials are a plus, and a Bachelor's degree is