Regulatory Affairs Supervisor

Regulatory Affairs Supervisor Full-time Workday Global Grade: 14 Company Description About AbbVie 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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description DEPARTMENT FUNCTION/OBJECTIVES The Regulatory Affairs Department obtains and maintains marketing approvals of responsible Abbvie products in Taiwan. It ensures full local regulatory and company compliance, and provides regulatory expertise to support clinical research, product launches, business development so as to assist achieving business growth and full compliance with legal requirements for pharmacovigilance regarding regulatory affairs relevant responsibilities. PRIMARY FUNCTION/OBJECTIVE The position is to handle preparation of regulatory submissions in order to obtain and maintain marketing approvals of company products, and to provide advice on regulatory matters to staff and customers. CORE JOB RESPONSIBILITIES Manage registration of new products and variations to marketed products to ensure regulatory approvals are achieved in accordance with company objectives. Ensure new product registrations and approval maintenance is conducted in a timely manner according to the registration plan, with guidance from RA manager where required. Coordinate responses to deficiency letters and other requests for data from regulatory authorities for products and ensure it meets agreed or required timelines. Liaise with officials of government agencies to facilitate evaluation processes and respond to requests for data in agreed timelines. Update product labeling in a timely manner based on the update of the product labeling from headquarters. Review labeling and product information to ensure compliance with relevant regulations and codes. Generate registration plans and provide regular status reports.Report progress and status to manager and management as required including to corporate RA and NPI meetings. Communicate regulatory issues and evaluate the impact on the business to RA director, senior management and Business Unit, and to GM where applicable, under the supervision of RA manager. Maintain good knowledge of relevant corporate policies and local regulations and ensure compliance. Keep abreast of regulatory changes and evaluate the impacts on the business and communicate changes in a timely manner to related parties and management. Update RA SOPs when regulations and processes are updated and review them to ensure they are within the validity timeframe. Participate in RA process and streamline processes to increase productivity. Other regulatory projects and tasks assigned by RA Director/Senior Manager/Manager/Associate Manager. Qualifications University degree in Pharmacy, Pharmacology, Biology or related disciplines Minimum 3 years’ experience and in-depth knowledge of Taiwan Regulatory in new drug applications for NCE Good communications and coordination skills Strategic and analytical thinking Proficiency in communicating strategic and tactical issues Proven interpersonal skills Additional Information AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html By clicking the link above or any