Regulatory Operations Executive

Responsibilities:

• 1 to 3 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.