Senior Regulatory Affairs Professional

7 days ago

davangere, India beBeeRegulatoryAffairs Full time

Regulatory Affairs ExpertiseAs a seasoned Regulatory Affairs Specialist, you will be responsible for handling the complex and multifaceted world of regulatory submissions. Your role will involve navigating the intricacies of global health authorities, ensuring compliance with regulatory requirements, and managing end-to-end preparation and submission of ANDA, NDA, BLA, MAA, and other lifecycle submissions.Key Responsibilities:Author, compile, and submit regulatory dossiers to global health authorities, including USFDA, EMA, MHRA, TGA, HSA, NPRA, Thai FDA, Taiwan FDA, CDE, NMPA, PMDA, and others.Conduct dossier gap analysis to identify document and data gaps across all CTD modules (1–5).Convert and prepare dossiers in multiple formats including eCTD, ACTD, and CTD.Manage end-to-end preparation and submission of ANDA, NDA, BLA, MAA, and other lifecycle submissions (variations, renewals, withdrawals).Coordinate responses to health authority queries through cross-functional collaboration and data collation.Maintain a strong command over CMC, clinical, non-clinical, and administrative documentation to ensure successful global submissions.Project Planning & ManagementAs a key member of our team, you will be responsible for managing regulatory submissions for multiple products across multiple countries simultaneously. This will require utilizing project management tools to track project milestones, timelines, and deliverables, as well as ensuring efficient time and resource allocation to meet submission deadlines.Manage regulatory submissions for multiple products across multiple countries simultaneously.Utilize project management tools to track project milestones, timelines, and deliverables.Ensure efficient time and resource allocation to meet submission deadlines.Foster seamless communication between central regulatory, regional teams, and client stakeholders.Requirements:To succeed in this role, you will need to possess the following skills and qualifications:8–10 years of core experience in Regulatory Affairs, handling submissions across regulated and RoW markets.Strong understanding of global dossier formats, submission pathways, and lifecycle management.Excellent cross-functional communication and coordination skills.Proven ability to manage complex multi-country regulatory portfolios.

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