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We're Siemens, a global innovation company helping the needs of businesses, communities and employees right here in the US. From improving security at airports, to helping healthcare professionals make more accurate diagnoses of the heart, to reducing delivery time for forwarded mail and beyond, we're achieving the unexpected all because of our employees. Which is why we offer a work culture where ideas are free to fly, diversity programs that capture the strengths of thought rather than ethnicity, and mentoring and training programs that can take careers to new heights. And that's pretty inspiring.
Because when you and 70,000 diverse minds innovate together, you can change the world. Imagine that.
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Siemens is an equal opportunity employer encouraging diversity in the workplace.
Software Quality Assurance
Company: Siemens Healthcare Diagnostics Inc.
Division: SMSD - IVD OPS
Location: MA - Norwood
Req ID: 83811
Position Title: Software Quality Assurance
Experience Level: Mid Level
Education Required: Bachelors Degree or equivalent experience
Travel Required: Yes
Company Description:
Siemens Healthcare Diagnostics Inc. offers a broad portfolio of performance-driven diagnostic solutions that provide more effective and efficient ways to anticipate, diagnose, monitor and treat disease. Our products and services offer the right balance of science, technology and practicality across the healthcare continuum to provide medical professionals with the vital information they need to deliver better, more personalized healthcare to patients around the globe. Visit us at www.siemens.com/diagnostics .
Siemens is an Equal Opportunity Employer encouraging diversity in the workplace.
Job Description:
Perform software verification activities as a part of the overall software development process. The primary
responsibilities of the validation engineer are to:
- Verify through testing or inspection that the product functionality meets the software requirements
- Creating software validation test scripts and executing these scripts to verify design meets intended requirements
- Plan and implement configuration of physical setup of equipment
- Record, in writing, all tests and planning sessions
- Inducing system errors to verify software behavior is as defined in the specification
- Create/track software defects in the defect tracking database and verify closure of defects
- Report passed and failed requirements to validation lead and project team and manager
- Communicate task status in writing to the validation lead and manager
- Interact with validation and development personnel on a project
Must have knowledge of how software verification / validation activities integrate within a software development process.
Knowledge of any of the following items is a plus:
- FDA Design Control regulations
- Various programming languages, such as C ++, C or Visual Basic
- Communication protocols, such as LIS 3, HL7
- Automated testing tools, such as QTP
- Chemistry
- Calculated Parameters for Blood Gas analytes
- Corrections using slope and offset
- Statistical Data Analysis
- Experience with medical devices
The validation engineer skills include:
- Black-box, performance, back -end, stress and load testing, as required
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Additional Information:
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