Regulatory Affairs Analyst - This role plays a key part in supporting new product registrations, post-marketing activities, and regulatory strategy execution within the pharmaceutical domain. Key Roles & Responsibilities- Prepare, review, and submit high-quality CTD dossiers for new drug product registrations and post-marketing variations in compliance with regulatory requirements. - Prepare and respond to Deficiency Letters issued by ANVISA, ensuring timely and accurate submissions. - Conduct …