AVVA Pharmaceuticals: Regulatory Affairs Manager – Limassol
AVVA Pharmaceuticals is currently recruiting for the position of
Regulatory Affairs Manager
The Regulatory Affairs Manager is responsible for the planning, publishing (paper, NeES, eCTD), construction, review and delivery of regulatory submissions to global Health Authorities within required time frames.
The primary accountability for this role is focused on new submissions.
You will need:
- Bachelor’s degree is required, Pharmacy, Chemistry, Biology
- 3 years of pharmaceutical experience in a global regulatory environment, including experience with document management technology and electronic publishing software (e.g. Documentum, FirstDocs, ISI Toolbox, eCTDXpress, etc.).
- Excellent command of English language, other languages will be considered as an advantage
For more information please contact us at firstname.lastname@example.org or at +357 25572200.