Job Purpose: Ensure product registrations, tender preparation, regulatory compliance, and product quality in Taiwan.Main Tasks: Set up a good registration strategy to drive new products speed to market.Market continuity of registered products through efficient maintenance and renewal of licenses and tender submissions.Compliance to quality and regulatory requirements defined by local authorities and S&N policies.Management of post-market activities to ensure patient safety, product quality, and regulatory compliance.Establishment and management of relevant quality processes and practices to meet competent authority and company expectations.Ensure compliance with current and new regulations and guidelines within Taiwan for Regulatory Affairs.Maintain good working relationships with competency authority in the region and seek to influence appropriately, with the aim of achieving optimal registrations with minimal delay.Participate in cross-functional team activities from initial stages through securing government approvals.Support the company in identifying and eliminating regulatory risks.Optimize cross-functional support needs in the company, ensuring effective communication with the Medical, Marketing, and Sales Teams.Other RAQA activities, including but not limited to local labelling, OTC pack, GDP, post-market activities, UDI, and import permit.Supplementary Tasks: Conduct review of promotional materials.Proofreading or minor translations of English sections.Job Requirements: 3 years or above relevant experience (less experience will also be considered).Fluent oral and written skills in English.Strategic thinking and planning.Effective negotiation and influencing.Clear and actionable communication.Accurate sense of urgency, prioritization, and delegation.Updated and comprehensive knowledge of local regulations, and ability to translate them into actionable strategies. #J-18808-Ljbffr