Role Responsibilities:

• 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.

Skills and Experience

• Science, computer science or engineering degree

• Min 1 year of experience in pharmaceutical industry / Medical Device / any related industry (preferably relevant experience in regulatory affairs will be an advantage)