Opportunity Description
Summary:
Provides technical and quality system guidance related to establishing product software as a medical device requirements.
Provide quality oversight for product software as a medical device verification and validation activities for new products in accordance with design planning procedures. This includes, but is not limited to, reviewing and approving software test case protocols and reports, review of software development plans, and review of other system and software documentation.
Product software as a medical device – verification and validation activities for new products (Quality Engineer supporting the R&D team). Roles and Responsibilities:
Leads meetings to prioritize, review and/or approve of action plans for addressing issues captured in problem resolution systems during development.
Leads risk evaluation and associated management activities related to product software development includ...
Full-time
Engineers