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Senior Software QA & Requirements Coordinator

  • 2024-35468
  • Rishon Le Zion, Israel
  • 研究開発
  • ハイブリッド

Job Description: 

We are looking for an experienced Software Quality Assurance Specialist with strong Business Analysis skills to join our team. In this dual role, you will lead quality assurance efforts while taking a proactive role in defining, analyzing, and reviewing product requirements for software applications used in clinical diagnostic instruments, ensuring quality, compliance, and seamless functionality essential for clinical settings. 

Key Responsibilities: 

  • Software Quality Assurance: 
  • Develop, execute, and document comprehensive test plans and test cases to verify software functionality, performance, and compliance with industry standards and regulatory requirements. 
  • Create test cases, validation plans, and traceability matrices specific to clinical and medical applications. 
  • Manage bug tracking and oversee testing for compliance, usability, and performance for software interacting with diagnostic hardware. 
  • Work with cross-functional teams to troubleshoot and resolve issues, ensuring high-quality standards throughout the development lifecycle. 
  • Monitor and report on testing progress, and provide clear documentation of results, including defect tracking and resolution. 
  • Business Analysis: 
  • Define, document, and manage software requirements based on stakeholder input and regulatory needs, maintaining clear alignment with project goals. 
  • Analyze and interpret complex business needs, translating them into detailed functional and technical specifications. 
  • Facilitate cross-functional collaboration, ensuring development and quality assurance are integrated with regulatory requirements and client expectations. 

Qualifications: 

  • Bachelor’s degree in a relevant field (e.g., Biomedical Engineering, Computer Science, Clinical Diagnostics). 
  • Proven experience (5+ years) in software quality assurance, ideally with medical or clinical diagnostic applications. 
  • Strong background in requirements gathering, analysis, and documentation. 
  • Knowledge of regulatory compliance in the medical field (FDA, ISO) and risk management processes. 
  • Excellent analytical skills, attention to detail, and experience with SQA tools and methodologies. 
  • Proficiency in English; other languages are an advantage. 

Preferred Skills: 

  • Experience and familiarity in automated testing tools such as QTP and Ranorex. 
  • Experience with requirement management tools and quality management systems (e.g. JIRA, Jama, Azure DevOps Test Plans, MTM). 
  • Prior work with medical devices or diagnostics companies. 
  • Certifications in Quality Assurance (ISTQB) or Business Analysis (CBAP) are a plus. 

 

Legal Entity: (ISR_2036)Bio-Rad Israel Ltd

 

 

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