Job Title: Quality Assurance Engineer
Date Posted: 03-18-2008
Job Location: California-Silicon Valley/San Jose
Job Type: Full Time
Education Level: Bachelors Degree
Work Experience: 2+ to 5 Years
Job Shift: First Shift
Yearly Salary:DOE (Depend on Experience)
Company Name: NeuroPace, Inc.
Contact Information: NeuroPace, Inc.   NeuroPace, Inc. (hr@neuropace.com)
Job Description:
Responsibilities:

1.      Provide quality engineering support for new electro-mechanical and software product
development and design change efforts through participation on project teams. Perform the
following types of tasks as assigned:

         Participate in development of schedules, deliverables including requirement
specifications (i.e., MRS, PRS, SRS) 

         Perform safety and/or reliability analyses

         Perform process and design FMECAs, FTAs, Risk Analyses

         Prepare design verification plans, participate in testing, review design
verification and validation protocols and reports

         Plan, document and conduct component verification and validation  

         Participate in design for manufacturability analyses and reviews; conduct
engineering tests and perform DOEs

2.      Participate in process development, validation, and improvements through the conduct
of testing, reporting and/or review of data and reports

3.      Provide statistical analysis guidance for sample size determinations, evaluation of
test results, quality system improvements, etc. 

4.      Support new and ongoing manufacturing efforts, including supplier management,
inspection and test of components and assemblies, disposition of discrepant materials;
participate on engineering change board for design and manufacturing changes

5.      Assist with resolution of product and process defects as determined through failure
analysis, focusing on root cause analysis and implementation of effective corrective action 

Requirements:

1.      Minimum of BS degree in Materials or Electrical Engineering and 1-3 years experience
in a development or manufacturing environment

2.      2-5 years medical device or automotive experience a plus

3.      Familiarity with ISO 9001:2000, ISO 13485:2003, QS-9000 and/or FDA Quality System
Regulations desirable; a working knowledge of the application of safety standards to high tech
development a plus 

4.      Demonstrated attention to detail and excellent interpersonal skills, both written and
verbal, are essential
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