Category
Financial Services
Description
Role Responsibilities:- 1 to3 years of experience in pharmaceutical industry / Medical Device / any related industry (preferably relevant experience in regulatory affairs will be an advantage)
- 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' 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.
Job ID: 81274298
