Regulatory Affairs Manager

PRIMARY FUNCTION/OBJECTIVE The position is to handle preparation of regulatory submissions in order to obtain and maintain marketing approvals of company products, to provide advice on regulatory matters to staff and customers and design RA strategy and lead cross functional meeting. RESPONSIBILITIES Independently manage registration of new products and variations to marketed products (including medical devices) to ensure regulatory approvals are achieved in accordance with company objectives. Ensure new product registrations including BSE submissions and approval maintenance is conducted in a timely manner according to the registration plan. 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. Design RA strategy and lead cross functional meetings. Independently manage development projects, including early pipeline products, from RA perspective. Communicate regulatory issues and evaluate the impact on the business to RA director, senior management, Business Unit and GM where applicable. 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. Lead the team in the management of the regulatory projects Manage the performance of team members Other regulatory projects and tasks assigned by RA Director. University degree in Pharmacy, Pharmacology, Biology or related disciplines About 8 years’ experience and in-depth knowledge of Taiwan Regulatory in Medical Device or Pharmaceutical Industry. New drug applications for NCE and clinical drug development knowledge will be an added advantage. Strong communications and coordination skills Proficiency in communicating strategic and tactical issues to management Proven interpersonal skills Excellent oral, written and good computer communication skills, including fluent English. 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 US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: 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 . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.