Engineer I, Software Quality

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🕒 vor 3 Tagen

🇺🇸 Vereinigte Staaten – Remote

⏰ Vollzeit

🟢 Junior

🟡 Mittelstufe

👷🏻‍♀️ Ingenieur

👻 Geisterscore 10%

infoinfo

🗣️🇺🇸🇬🇧 Englisch erforderlich

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Logo of FUJIFILM Corporation

FUJIFILM Corporation

10.000+ Mitarbeiter

Gegründet 1934

🏭 Fertigung

🏥 Gesundheitswesen

Manufacturing • Healthcare • Electronics

Die FUJIFILM Corporation ist ein globales Unternehmen, das 1934 gegründet wurde und in verschiedenen Bereichen tätig ist, darunter Gesundheitswesen, Elektronik und Bildgebung. Als umfassendes Gesundheitsunternehmen entwickelt FUJIFILM ein breites Spektrum an Geschäftsfeldern in den Bereichen Prävention, Diagnose und Behandlung. Darüber hinaus legt das Unternehmen großen Wert auf ökologische Nachhaltigkeit durch verbesserte industrielle Effizienz und bewahrt Erinnerungen durch Film und Fotografie, bereichert emotionale Leben und menschliche Verbindungen.

Beschreibung

• Learn and become proficient in the Synapse Select product line, including on-premise and cloud deployment methods and architecture • Assist in creating and executing manual software test cases for Verification and Validation protocols • Perform occasional exploratory functional testing and ticket issues found • Reproduce and document product defects and reported bugs in JIRA • Execute development-ticket and regression testing with clear documentation of test results • Correspond with Software and Template Engineering and provide feedback or facilitate additional information • Participate in contractor QA team calls to groom development tickets and increase product knowledge • Participate in automated testing team calls to review implementation of new test cases • Create and design forms required by the Medical Informatics Design Control Process • Assist the Medical Informatics documentation team with service manuals and product documentation • Assist Operations and Support with technical questions about the Synapse Select product line • Perform additional responsibilities as defined by management • Comply with applicable medical device regulatory, ISO 13485, legal, regulatory, and standards requirements

🎯 Anforderungen

• Bachelor's Degree (B.S./B.A.) or equivalent work experience in a scientific or technical discipline • 0 to 2 years of experience in Software Development, Software QA or other related fields • Practical experience or knowledge about Software Development, testing, or Software QA • Basic knowledge of software medical devices, procedures, and terminology, including the DICOM standard and HL7 • Basic knowledge of AGILE Software development and software design controls • Experience with Microsoft® Word, Excel, Visio, and Access or equivalent software • Strong interpersonal, verbal, and written communication skills • Detail oriented • Problem solving ability • Ability to multi-task • Highly organized • Usual office working conditions • Good manual dexterity • Ability to sit for extended periods • Ability to occasionally lift and/or move up to 10 pounds • Willingness to travel occasionally, up to 10% • Must comply with applicable U.S. FDA medical device regulatory requirements, ISO 13485 requirements, and other applicable laws, regulations, and standards • Must be willing to periodically test for COVID-19 and wear a face covering indoors as required, subject to applicable accommodations

🏖️ Vorteile

• Flexible work environment • Equal opportunities in hiring, promotion and advancement, compensation, benefits, and training • Reasonable accommodation during the application and selection process • COVID-19 vaccination accommodation for medical, religious, or other legally required exemptions • Vendor credentialing and facility vaccine requirement accommodations where legally applicable

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