Responsibilities:
- handle and oversee various regulatory procedures
- regulatory applications, labelling projects, medical translations
- co-ordination of projects
- communication with clients and respective health authorities
We expect from you:
- Masters degree in medicine, pharmacy or other life sciences
- Professional fluency in English and Latvian language
- Pharmaceutical regulatory Affairs experience
We offer:
- Possibility to work in home office with flexible schedule.
- supportive colleagues
Lithuania
Estonia
Slovenia
