We are seeking a Regulatory Affairs Executive with 1 to 3 years of experience in the pharmaceutical industry.
The ideal candidate should have hands-on experience in compiling and reviewing ACTD and CTD dossiers for various regulatory submissions.
Responsibilities include preparing, compiling, and maintaining regulatory documentation in accordance with regional requirements, coordinating with cross-functional teams to gather necessary data, and ensuring timely submission of dossiers.
The candidate should be well-versed with regulatory guidelines, and capable of handling multiple projects simultaneously.