PUESTO CERRADO

CONFIDENCIAL
Publicación | 2023-10-27 |
Finalización | 2023-11-10 |
Tipo Vacante | Vacante |
Quality Inspector I
QualityResponsible to the product inspection at all stages (incoming, in process, FG, shipping), and product release. Also support validation activities, quality reporting, process auditing activities, investigation of exceptions and supporting change control actions.
Roles y Responsabilidades
Inspect incoming materials:
- Coordinate with engineers to define critical inspection criteria
- Set up inspection files
- Perform first article inspections
- Determine correct sample size
- Document non-conformances to specifications
- Investigate and report nonconforming product events
- Segregate and Dispose of nonconforming materials and product
o Provide support on SCAR’s Management System.
Provide support to the following functions:
- Perform in-process and final inspection, when deemed necessary.
- Supplier Quality Management (supplier files and performance, SCARs, ASL)
- Quality Compliance Engineering.
Educación / Experiencia
· High school diploma or general education diploma (GED).
· 3 years’ work experience in a similar positions preferable medical devices industry
Habilidades y Competencias
· Excellent communication skills, and problem solving skills.
· Detail oriented.
· Basic knowledge of metrology.
· Ability to plan and schedule multiple projects and tasks.
· Be able to work with people at all levels of organization
· Proficient with MS Office Word, Excel, Outlook - experience with using spreadsheets for management of data.
· Good written and oral communication in required.
· Must be willing and able to work and problem solve independently, as well as, part of a team
· Must be able to work within deadlines
· Must be a proactive, self-starter with a results-oriented focus.
· Must possess a “can-do” attitude, able to produce consistently accurate results at a fast pace, willing and capable of assuming additional responsibilities.
Requisitos
· Preferred experience with management of technical documentation
· Preferred experience in a manufacturing environment