Job Description

Position: Manager Development Quality Assurance

Location: ViewRay Systems, Oakwood Village, Ohio

About ViewRay Systems

ViewRay Systems, Inc. is a private technology company seeking to provide the global radiation therapy community with advanced medical instruments incorporating the highest level of technology possible. Our belief is that only significant technological innovation can enable society to conquer disease. Our mission is to dare to change the paradigms of medicine and solve “impossible” technical problems to enable clinicians to effect a cure to save precious human lives, mitigate pain and suffering, and enhance quality of life. Our vision is to become the world’s leader in producing highly effective innovative technology to cure cancer.

ViewRay Systems designs, manufactures, and markets the MRIdian A3i® radiation therapy system to treat cancer patients with the smallest radiation therapy margins available [i] with the highest patient throughput demonstrated for the most complicated cases [ii] The system treats by aligning the sharpest radiation therapy beam on the market to diagnostic quality magnetic resonance images (MRIs) of the patient, adapts the treatment plan to the reality of the patient, and then uses the real-time MRIs to control the beam and record real-time doses delivered to the patient.

Job Description

ViewRay Systems, Inc. is looking for a Manger/Senior Manager Development Quality Assurance that shares our passion for conquering cancer and help us support radiation therapy systems worldwide. The ideal candidate shares enthusiasm for engaging in the best business practices while improving cancer therapy. You will be leading with the development of software algorithm test suites, development of automated test suites, and integration of these algorithms within software subsystems.

Responsibilities include the following and other duties may be assigned

• Hire, train, and mentor software test engineers.
• Testing Strategy: Develop and implement testing strategies that adhere to regulatory requirements (e.g., FDA, IEC 62304).
• Test Planning: Plan and manage software testing activities, including test case development, test execution, and defect tracking.
• Regulatory Compliance: Ensure that all testing activities comply with current regulatory requirements for medical device software.
• Risk Management: Identify and mitigate risks associated with software testing.
• Collaboration: Partner with cross functional teams to ensure the successful delivery of medical device software.
• Process Improvement: Continuously improve software testing processes and methodologies.
• Documentation: Maintain accurate and comprehensive documentation of testing procedures, results, and findings.
• Create test procedures to evaluate the performance of software algorithms.
• Build software testing programs for new algorithms that automate testing processes.
• Run the software testing procedures to evaluate the software.
• Document all testing procedures.
• Report anomalies and make recommendations to improve the software product.
• Collaborate with other engineers, software developers, and other R&D scientists.
• Ensure compliance with product development design control processes including SDLC/IEC62304 and risk management.
• Maintain requirement quality, verification, and traceability.

Education, Experience, Skills

• Bachelor’s degree in computer science or a related engineering field (SW, ME, EE, IE) or equivalent.
• 3-5+ years of successful experience as a quality test engineer for similar products with a high degree of complexity.
• Extensive experience: Experience in software testing, especially in a regulated environment like medical devices.
• Technical knowledge: Strong understanding of software development lifecycle, testing methodologies, and regulatory standards.
• Leadership skills: Ability to lead, motivate, and manage a team of engineers.
• Communication skills: Excellent communication and interpersonal skills to work effectively with other teams.
• Problem-solving skills: Ability to identify and resolve technical issues related to software testing.
• Analytical skills: Ability to analyze test results and identify areas for improvement.
• Strong Technical Skills: Proficiency in software testing principles, methodologies, and techniques, including manual testing, test case design, and defect tracking.
• Programming Knowledge: Experience with programming languages such as Python, C++.
• Testing Automation: Experience with automated testing tools and frameworks.
• Experience configuring a variety of software operating systems (i.e., Windows, Ubuntu, MacOS) and various networking hardware products.
• Knowledge and experience with FDA & ISO13485 Quality System regulations, IEC62304 software development lifecycles (SDLC) and methodologies.

Personal Interactions

• Ability to communicate effectively, both orally and in writing, at a variety of technical levels.
• Ability to work effectively as part of the diverse team including physicists, scientists, and engineers in a fast-paced environment and with multiple projects.
• Able to travel up to 10% & lift 50 lbs.

Job Type: Full-time

Pay: Commensurate with experience

Ability to Relocate: Cleveland, OH 44128: Relocate before starting work (Required)

Work Location: In person in Cleveland, OH: Relocate before starting work (Required)

Benefits :

• Health, dental, and vision insurance
• Paid time off and flexible schedule
• Office stocked with snacks, drinks, and occasional catered meals

Email inquiries to careers@viewraysystems.com

ViewRay Systems, Inc. is an Equal Opportunity Employer and does not discriminate on the basis of race, religion, color, creed, national origin, gender, age, sexual orientation, status as a protected disabled or Vietnam Era Veteran, disability, or any other legally protected status.

[i] Kishan AU, Ma TM, Lamb JM, et al. Magnetic Resonance Imaging–Guided vs Computed Tomography–Guided Stereotactic Body Radiotherapy for Prostate Cancer: The MIRAGE Randomized Clinical Trial. JAMA Oncol. 2023;9(3):365–373. doi:10.1001/jamaoncol.2022.6558

[ii] Claudio Votta, et al. , Evaluation of clinical parallel workflow in online adaptive MR-guided Radiotherapy: A detailed assessment of treatment session times, Technical Innovations & Patient Support in Radiation Oncology,

Volume 29, 2024, 100239doi:10.1016/j.tipsro.2024.100239

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