Applicants must be eligible to work in the specified location
Tools:
- Microsoft Office; Minitab, Reliasoft or other statistical packages. SAP and LabVIEW knowledge a plus.
Description:
- Execute requirement analysis, V&V planning, V&V protocol and V&V report writing.
- Maintain, validate and release Test Reports for design changes, ideally in FDA regulated business.
- Firm understanding of product/design Verification and Validation, and Software Validation, requirements and practices.
- Familiarity with and ability to understand Medical Device Product Safety Standards (IEC 60601-1, et. al) and regulations (FDA CFR 820, EU MDD).
- Guide and participate in tracking of issues, including problem identification, testing, solving and
- verification/validation.
Wallingford Connecticut, United States of America
Richa Shetty
JS
12/19/2018 4:22:09 PM
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