| Date de publication | Type de poste | Lieu de travail | Expérience | Étude | Disponibilité | Langues | Mobilité |
| 12 avril 2022 | CDI | Cite El Khadra, Tunis, Tunisie | Moins d'un an | Bac + 5 | 1400 – 1700 DT / Mois | Plein temps | Français , Anglais |
Description de l’annonce:
In the context of a new project for one of our top Pharma client, we’re looking for a talented consultant to lead the following missions, and much more!
- Compile, or supervise the compilation of regulatory dossiers in accordance with national requirements
- Gain regulatory authority approval
- Provide on-going regulatory advice to project teams to ensure regulatory concerns are planned and accounted for and the relevant data are generated to meet project objectives
- Provide regulatory support to clients and associate companies
- Liaise with external regulatory authorities as required
- Provide format and contents review of packaging texts, Summary of Product Characteristics, Patient Information Leaflets and labelling
- Review tasks for, support and mentor Regulatory Affairs Associates
Profile:
- Degree in Life Science/ Pharmacy degree would be a plus
- First experience in Regulatory Affairs in the Pharmaceutical industry
- Knowledge of Africa and/or MENA regulations for pharmaceuticals (NCE, Biologicals and Biotech)
- Excellent communication skills in English, French and Arabic
- Excellent attention to details
- Ability to work well within a multicultural team
- Good time management skills