About this role
Job Description Summary -Contributes and support the development of submission of product registration, progress reports, supplements, amendments, and/or periodic experience reports. Supports all registration activities of the Department to ensure compliance with the requisites of the local pharmaceutical regulatory environment. Job Description Major accountabilities Review pipeline and set the registration strategy in collaboration with global RA and related CPO functions with support from senior specialist and manager Achieve the best product registration with optimal label by conducting research on submission requirements and approval lead time in accordance with registration plan.
Support launches (artwork, barcode, Drug ID mark, etc.) Perform CTA and get approval to ensure study timeline in collaboration with other CPO functions. Support IMP management through confirmation of variant number. Maintain product license by managing variations for label, quality (CMC and mfg. site) and administrative changes according to local law/regulation/guidelines, company strategy and global compliance.
Secure product license by managing Reevaluation/Renewal/Reexamination /HA safety communication Ensure post approval activities (website, artwork, etc.) Submit RMP by supporting of other function in line with global direction. Be accountable for correct and timely update of RA compliance (registration) database (DRAGON) Ensure industry compliance with NP4, KRPIA code of conduct Support cross functional activities by delivering regulatory input Understand basic knowledge on the legal frameworks, internal processes, GxP’s Keep abreast of relevant laws /regulations and apply to related CPO activities Ensure reporting and follow up of all spontaneous adverse events (AE) and technical complaints for all Novartis products according to respective SOP Foster and maintain good relations with internal and external stakeholders. Communicate effectively with HA and other BFs Understand RA internal working process and handle own task well Essential Requirements Education: 4-year university degree, preferably in Pharmacy, Biochemistry, Chemistry, Life Sciences, or a related field Languages: Fluent in both written and spoken English Experience: Pharmaceutical industry experience preferred Knowledge: Basic understanding of regulatory affairs, drug development process, and applicable pharmaceutical regulations/guidelines preferred Skills Desired Clinical Trials, Collaboration, Detail-Oriented, Project Planning, Regulatory Compliance