Profile
- Chemical graduate or similar
- High English level essential. Computing skills
- Additional experience and knowledge in GMP´s will be valued
- Experience in similar position in the Pharmaceutical Chemistry Industry will be valued
- Methodical and organized person. Team work
Functions
- Manufacturing Records checking
- PQR´s writing
- Customer audits assistance
- Deviations, Change Controls, CAPA´s management
- CDMO projects collaboration