We are currently growing our local Regulatory Affairs team and looking for:
- 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.
- Science, computer science or engineering degree
- 0 - 1 year of experience in pharmaceutical industry / Medical Device / any related industry (preferably relevant experience in regulatory affairs will be an advantage)
- Knowledge of Regulatory processes and related tools will be an advantage
- Computer literacy is essential
- Excellent verbal and written communication skills in English
- Demonstrated ability to be innovative and a creative thinker
- Opportunity to be a part of a rapidly expanding, well known global organization
- Role that allows you to progress both professionally and personally
- Diverse and multinational environment
- Friendly and inspiring work atmosphere
- Trainings with international specialists
- Excellent location and office space
- Competitive salary and benefits
Poznaj
Cognizant
Cognizant (Nasdaq: CTSH) is an AI Builder and technology services provider, building the bridge between AI investment and enterprise value by building full-stack AI solutions for our clients. Our deep industry, process and engineering expertise enables us to build an organization’s unique context into technology systems that amplify human potential, realize tangible returns and keep global enterprises ahead in a fast-changing world. See how at www.cognizant.com or @cognizant.