Job Title Regulatory Affairs Associate - Regulatory Information Management RIM - UST Band B1 Role detailed classification RIM Regulatory Information Management Job Summary We are seeking highly skilled and experienced Life Sciences LS Regulatory Affairs RA Associate - RIM to join our LS Practice team The successful candidate will be responsible for LS Regulatory Information Management RIM and or other assigned RA activities The role will involve knowledge of Global Regulatory Affairs guidelines platforms and systems to undertake various assigned roles and responsibilities included but not limited to below described activities Key Responsibilities Life Sciences Regulatory Affairs Associate - RIM plays a crucial role in ensuring compliance within the pharmaceutical medical devices and biotechnology industries by managing the assigned regulatory affairs RIM activities for regulatory submissions health authority queries approvals variations renewals licence maintenance regulatory compliance throughout the product lifecycle This role involves preparing and reviewing regulatory information maintaining compliance with global standards and regulations and utilizing Regulatory systems to track and organize critical data for various assigned activities Specific RIM activities 1 Regulatory Information Management RIM Utilizing the assigned RIM system s to manage and maintain regulatory information track submissions health authority correspondence and approvals across regions and functions Support data migration configuration validation and user acceptance testing UAT 2 Maintain and update regulatory data in RIM systems e g Veeva Vault ArisGlobal EXTEDO etc to ensure accuracy completeness and compliance 3 Support regulatory submissions by coordinating data entry document tracking and metadata management 4 Collaborate with cross-functional teams Regulatory Affairs CMC Clinical Safety to gather and validate submission-related information 5 Monitor regulatory changes and ensure tim