Regulatory Affairs Specialist

We are seeking a Regulatory Affairs Specialist to join our team in Maharashtra. The ideal candidate will play a crucial role in ensuring that our products comply with all regulatory requirements. This position involves preparing and submitting regulatory documents, including Common Technical Documents (CTD) and electronic Common Technical Documents (eCTD), to health authorities. The Regulatory Affairs Specialist will work closely with cross-functional teams to gather necessary information and ensure timely submissions. Key responsibilities include maintaining up-to-date knowledge of regulatory guidelines, preparing regulatory submissions, and liaising with regulatory agencies. The candidate should possess strong analytical skills, attention to detail, and the ability to work under tight deadlines. Familiarity with the regulatory landscape in the CIS region is a plus. Required skills for this role include expertise in regulatory affairs, dossier preparation, CTD, eCTD, and drug regulatory affairs. If you are passionate about regulatory compliance and want to contribute to the success of our products, we encourage you to apply.