**Key Areas of Accountability:** **1. Submissions and Approvals** a) Dossier Preparation Prepare a quality regulatory dossier for Food/Nutritional, Drugs, Medical Device products and submit within the planned affiliate timelines. (manages majority of major brands’ initial registration, License to Operate Initial Application or variations, promo permit submission) + Request and obtain the various regulatory items needed for the local submission + Prepare/format the dossier to ensure it meets local requirements + Review labelling materials in to comply with the necessary regulation, as applicable + Implement the submission and archive appropriately b) Gain Regulatory Approval Gain Food and Drug Administration (FDA) or respective regulatory agency approvals to meet the affiliate product launch plans and ensure product maintenance. + Provide quality responses to the FDA on or before the due date + Complete regulatory approval process and gain product licenses. + Communicate Product approval + Archive submission dossier and approval documents + Perform regulatory responsibilities related to label and packaging development (Reviewer in Prima or DevEx systems, provides input on regulatory information and supporting documents required for label development) + Ensure the local label creation and packaging development will meet local and corporate criteria and supports the business needs c) Metrics Review Prepare monthly Regulatory Report of status monitoring and communicate to local management. d) Regulatory Lead for NPI and Project Meetings Ensure knowledge and understanding of the on-going regulatory projects and manage launch requirements with cross-functional team. **2. Regulatory Lifecycle Compliance** a) Compliance Maintenance Take appropriate actions to maintain all local marketed products in compliance with local and corporate regulatory requirements Conduct compliance self-audit to identify potential compliance issues Complete Global and/or Regulatory Core Curriculum system trainings **3. Regulatory Influence** a) Regulatory Customer Relations Keep abreast of regulatory updates, changes and trends affecting local regulations which could impact business environment and communicate appropriately with affected parties. b) External Engagement To maintain and strengthen communication with appropriate offices of the Food and Drug Association (FDA) and industry associations **Knowledge & Experience:** + Minimum 8-year experience in performing regulatory affairs responsibilities from the Food Industry, Medical Device and/or Pharma. At least 4 years are performed in a supervisory/specialist level. Preferably with Food and Food Supplement evaluation and submission experience with the Ph FDA + Have in-depth knowledge of FDA-Center for Food Regulation and Research regulations pertaining to product registration and related submission activities (eg but not limited to promo applications, import permits) **Professional Competencies required:** + Knowledgeable in the operation of Microsoft Word, Excel, Powerpoint and Adobe Acrobat Professional; + Good knowledge of written and spoken English + Strong and competent project management and organization skills + Ability to handle and multi-task activities + Analytical skills: accuracy, reliability, attention to detail **Minimum Qualification:** Graduate of: Bachelor's degree (or equivalent) is required - preferred area of focus in science (Nutrition, Food Technology, Pharmacy, Industrial Pharmacy) An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com