Обязанности:
- handle and oversee various regulatory procedures
- regulatory applications, labelling projects, medical translations
- co-ordination of projects
- communication with clients and respective health authorities
От Вас ожидаем:
- Masters degree in medicine, pharmacy or other life sciences
- Professional fluency in English and Latvian language
- Pharmaceutical regulatory Affairs experience
Мы предлагаем:
- Possibility to work in home office with flexible schedule.
- supportive colleagues
Литва
Эстония
Словения
