Vacancy expired!
- Progresses investigations and other activities through the CAPA program.
- Leads cross-functional teams in the use of investigational tools to determine the root cause of nonconformities, ensures that CAPA plans address root causes, and that CA/PAs are implemented timely to facilitate the rapid and compliant introduction of new/improved products, processes, and systems.
- Ensures that actions are on time, thorough, complete, and meet the needs of the business and customers, and that required standards and/or procedural requirements are met.
- Leads a multifunctional team, ensuring that all communications, interpersonal interactions and business behaviors are consistent.
- Knowledge of the Corrective and Preventative Action process in medical devices
- Understanding of statistics
- Experience with medical devices which have reagents, complex electro-mechanical and optical components.
- Bachelor of Science in a life science or engineering discipline
- Engineering Degree
- Experience in Quality Engineer/Medical Device
- 2 to 4 years experience
- Need to have technical process
- Very good communication - verbal and written
Vacancy expired!