Quality Engineer to serve as primary QA personnel, supporting the day to day manufacturing operations in AVPR.
Responsibilities:
- Investigations QE and ME service engineer to address all the opportunities found in the assigned manufacturing line.
- QA management representative in the manufacturing line, executing initiatives and working directly with the DL workforce.
- Oversight of procedural readiness execution and remediation, measuring execution and effectiveness, track all quality improvement actions and projects in the area, monthly reporting on quality improvement activities, ownership of Quality Improvement projects (initiating Change Request / Change Order as necessary and overseeing the change was implemented and sustainable), and support to Investigations Engineers.
Requirements
- BS in Engineering
- Minimum of 2 years of relevant experience in Quality and/or Compliance, preferably in medical device industry
- Knowledge of applicable US non-US applicable regulations.
- Bilingual (Spanish/English)(Writen/Spoken)
BS in Engineering Minimum of 2 years of relevant experience in Quality and/or Compliance, preferably in medical device industry Knowledge of applicable US non-US applicable regulations. Bilingual (Spanish/English)(Writen/Spoken)