Johnson & Johnson Careers
Senior Manufacturing Engineer CDD
Requisition ID: 1905725309W
Job: Document process and equipment validation, Document machining process and instruction for production, Collaborate with quality engineering department. Address compliance issue and deliver strong investigation documentation.
Main tasks :
- Define the URS equipment ;
- Track process and equipment validation activities.
- Equipment installation
- Document and support IQ-OQ-PQ activities
- Document machining process and instruction for production.
- Collaborate with quality engineering département
- collaborate with US EMEA & ASIA sister companies
- Engineer, master degree, or Bachelor degree with strong experience in validation.
- Knowledge of IQ, OQ, PQ processus is required
- Experience with equipment installation is required
- A fair English level ( both speaking and writting ) to manage international exchange required.
- Microsoft office knowledge is required.
- Knowledge of medical device industry is a bonus
- Team work behavior needed
- Experience in PLM system is a bonus
Medos Sarl (8575)