Investigate moderately complex manufacturing product quality and compliance issues (e.g., CAPA, non-conformances, audit observations) for all production processes prior to final product release based on engineering principles; analyze results, make recommendations and develop reports.
Responsible for quality engineering activities, to monitor and measure compliance with the Quality System Regulation, Quality policies, FDA and ISO regulations as well as product quality and compliance objectives.
Complete part approval packages according to the customers unique requirements (e.g., create inspection standards, 1st articles, packaging drop tests, reliability tests, etc.). Requires interface with design groups.
The SQE works with our stranders and outside vendors to continuously improve performance through driving and facilitating problem solving, implementing process controls, promoting risk mitigation, and developing quality assurance plans.
Help programs resolve issues, etc.In this context, and working with ViaSats diverse and varied set of programs and products, our EQA engineers are constantly provided with challenges and opportunities to continual improve engineering quality.
Responsible for developing test methods and quality inspection procedures, developing and executing equipment IQ / OQ / PQ protocols and reports, conducting test method qualifications and validations, and creating sampling plans for incoming materials and in - process and finished product testing.
In this role, the selected candidate will design and implementing in house web applications test tools; update and maintain current test framework and create new feature tests with focus on cross product coverage.
In this role, you will be responsible for development and validation of supplier for Nitinol stent component processing (laser cut, heat setting, passivation processes)
Development and validation of inspection/measurement methods for challenging geometries and tolerances.