Junior/Senior Regulatory Affairs Specialist

• Be a part of a Team of dedicated professionals supporting critical pharma business process  
• Manage all aspects related to the preparation, tracking, compilation, publishing and technical quality control of all assigned regulatory submissions
• Ensure adherence to internal standards and processes, as well as Health Authority’s requirements.
• Report on submission progress
• Identify issues and solutions relating to timing, quality and resources

• Degree in pharmacy, chemistry,  biotechnology or related science
• Minimum 2-years of experience in registration processes of medicines, medical devices or other work in pharmaceutical company for Senior role
• Good understanding of pharmaceutical industry and drug registration processes
• Excellent technical skills (computer literacy)
• Excellent communication and interpersonal skills
• Analytical mind and eye for detail
• Team player
• English language skills and high level of organizational awareness

Experience in document publishing, eCTD lifecycle compilation and working in multinational organization will be a huge advantage.

• 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

In case this offer does not match your profile but you know someone who might be interested we would be grateful for forwarding this job offer!