Responsible for global regulatory submission / dossier publishing day-to-day activities and deliverables.
Compilation and maintenance of regulatory documentation as per the procedure in client repository.
Performing high level of files\xe2\x80\x99 formatting using the client provided software (creating bookmarks, hyperlinks, file optimization etc.).
Performing peer-review of work and providing support to other regulatory related activities as per the business requirements.
Interacting with relevant stakeholders during preparation and quality control of reports and regulatory documentation.
Skills and Experience
Bachelors in science, Computer science or engineering degree
1-2 year of experience in pharmaceutical industry / Medical Device / any related industry (preferably relevant experience in regulatory affairs will be an advantage)