Junior Regulatory Affairs Specialist

morning/evening shift

• 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.
• Following established processes and procedures and adhering to Client work instructions and procedures
• Self-motivation
• Achievement building orientation
• Relationship building
• Punctuality (self-discipline)

Essential Qualifications

• 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)

Essential skills

• Knowledge of Regulatory processes and related tools will be an advantage • Computer literacy is essential
• Excellent verbal and written communication skills
• Demonstrated ability to be innovative and a creative thinker

• Cooperation with the most incredible team you ever met
• Opportunity to be a part of rapidly expanding and well-known global organization
• Role that allows you to progress both professionally and personally
• Diverse and multinational work environment
• Inspiring work atmosphere
• Excellent location and office space
• Competitive salary and benefits