Regulatory Affairs Specialist (M/F)  

• Empresa Tecnimede Group - Ver mais ofertas

Tecnimede Group is a Portuguese multinational company, with more than 40 years of history in the life cycle of the drug product for human use - development, production, promotion and marketing - with the mission to improve and preserve the human life and the human health. […]
- Collaborate with internal teams in the pre-authorization phase (pharmaceutical, analytical and clinical development, and quality) and in the post-authorization phase (industrial production, pharmacovigilance, logistics, price and reimbursement and quality). […]
-Develop and update locally controlled regulatory documentation...

4 dias atrás De: expressoemprego.pt