- Braine L'alleud, Walloon Brabant, Belgium
- Hybrid
- Full-time · Mid
- 3+ years
Responsible for qualification of production systems and equipment, validation of manufacturing and cleaning processes, and maintaining regulatory compliance in a pharmaceutical production environment.
Responsibilities
- Define qualification and validation strategies based on risk analysis
- Write validation plans, protocols, reports and associated documentation
- Coordinate tests, track deviations and assign qualified or validated status
- Conduct periodic reviews and ensure compliance deadlines are met
- Maintain procedures and contribute to process improvement
Requirements
- Bachelor's or Master's in sciences, engineering or related field