<p>AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.</p> <p>Job Description</p> <p>This individual is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. The Manager assists Regulatory Staff by identifying and gathering data needed to support filings, responses to inquiries, and registration maintenance to enable commercialization of products that are developed, manufactured or distributed to meet relevant US and Canada regulatory requirements. Advises on US/C region specific requirements and assesses R&D programs against region specific regulatory requirements.</p> <p>Responsibilities:</p> <ul> <li>Responsible for a product(s) within Neuroscience and supports the Manager (Senior Manager, Associate Director, Director (Global Regulatory Lead (GRL)), in the development and execution of the regulatory strategy. Assigned matters may have an impact on business activities and operations. </li><li>Serves as Health Authority (HA) liaison with FDA for routine communications in support of filings including complete and timely responses during application review. Advise internal customers who may contribute to regulated communication on Regulatory/FDA issues including Public Affairs, Clinical Development, Legal, and others such as Commercial. Functions independently in negotiation and decision-making for project related issues that have cross-functional impact. </li><li>Key contributor responsible for the preparation and review of regulatory submissions consistent within US and Canada regulatory requirements and guidelines and assures complete and timely response to Health Authorities during application review. </li><li>Supports the regulatory submission and approval process. Applies regulatory/technical knowledge of government regulations and skills across therapeutic areas. </li><li>Recommends and implements changes to projects based on knowledge and expertise, accurate interpretation of US and Canada government regulations, guidance, as well as corporate policies and management-related considerations. </li><li>Presents pertinent regulatory information to appropriate cross-functional areas. </li><li>Operates in compliance with regulations, company policies, procedures, and guidance in alignment with regulatory product strategy and the Quality Dossier Program (QDP). </li></ul> <p>This opportunity is an onsite hybrid position located at AbbVie's Lake County, IL or Cambridge, MA offices.</p> <p>Qualifications</p> <ul> <li>Required Education: Bachelor's degree (pharmacy, biology, chemistry, pharmacology) or industry related. </li><li>Preferred Education: Advanced Degree a plus. Certifications a plus. </li><li>Required Experience: 6 years Regulatory, R&D, or Industry-related experience. </li><li>Preferred Experience: 2-3 years in pharmaceutical regulatory activities. </li><li>Skill Set: Proven skill at implementing successful US and Canada regulatory strategies, global regulatory experience is a plus. Experience working in a complex and matrix environment. </li><li>Skill Set cont'd: Good communication, both oral and written. Experience interfacing with government regulatory agencies. Demonstrates good negotiation skills and builds consensus. </li></ul> <p>Additional Information</p> <p>Applicable only to applicants</p>