CARDIVA MEDICAL – Sunnyvale, CA.
Job Title:
Engineer I / II, Process / Test Method Validation Engineering
Department:
Operations
SUMMARY:
Conducts process and test method development and
validations. Recommends, organizes and conducts
proof of concept for process improvements.
ESSENTIAL DUTIES AND RESPONSIBLITIES:
- With guidance from engineering
management, executes structured problem solving
and statistical process control to reduce
variation and drive continuous improvements in
final product quality, reliability and costs.
- Validates manufacturing processes for
new product development as well as commercial production
- Responsible for development and validation of Test Methods
- Responsible for working with R&D and
Operations to develop more efficient designs for manufacturability.
QUALIFICATIONS:
- B.S or M.S. degree in Engineering
(preferably mechanical or biomedical engineering)
EXPERIENCE / EDUCATIONAL REQUIREMENTS:
- Proficiency with Medical Device
development life cycles and manufacturing
processes and technologies is a plus, but not required.
- Knowledge of FDA regulations required, is a plus, but not required.
If interested, Please contact Justin Ballotta
(<mailto:justin_ballotta_at_cardivamedical.com>justin_ballotta_at_cardivamedical.com)
or Jennifer Lee
(<mailto:Jennifer_Lee_at_cardivamedical.com>Jennifer_Lee_at_cardivamedical.com)
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Received on 2011-06-21 06:16:17