Responsibilities
- Module-level design, implementation, and maintenance of high-quality software applications
- Maintain and improve existing image processing application
- Ensure successful integration of software modules in our larger software application suites
- Work with biologists, product management, software engineers, and mechanical engineers to define, implement, and verify software engineering requirements
- Participate in software engineering lifecycle from Planning, Analysis, Design, Implementation, and Reviews through testing and maintenance
Requirements
- Bachelor’s degree in computer science or engineering or a related technical degree
- 5+ years of industry experience
- 2+ years of experience in C# or Java
- Experience working with web-based distributed applications (Front-end / HTML / Javascript / CSS and Back-end REST-based APIs)
- Previous experience with image processing software development
- Experience with object-oriented programming and SOLID principles is required
- Experience with programming languages such as .Net /C#, Java, or C++
- Familiarity with the principles of SDLC and methodologies like Agile/Scrum, CI, Good Documentation Practices, Refactoring, and Testing Techniques
- Experience working with relational databases is preferred
- Strong analytical and debugging skills
- Openness to learning new tools such as C# 9.0 and the latest version of Angular
- Understanding of operating systems, especially Windows and Linux preferred
- Knowledge of static code analysis tools such as Coverity, SonarQube
- Experience with Microsoft Visual Studio and Azure DevOps preferred
- Desire to work in a fast-paced, collaborative start-up environment
- Experience in a regulated industry such as medical devices, cell therapy, bioprocessing, or instrumentation is highly desirable
- Self-awareness, integrity, authenticity, and a growth mindset
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What We Do
Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patients who can benefit. The clinical impact of cell therapy in treating cancer has been proven, but this therapeutic approach has several limitations, especially in manufacturing, leaving extremely sick patients waiting for treatment and desperate for hope. Since cell therapy is currently produced for a single patient at a time, it is expensive to manufacture, requiring significant time and resources, and is difficult to scale. Preclinical and clinical scientists, as well as commercial cell therapy manufacturers also lack the options to fully automate their manufacturing process quickly, safely, cost-effectively and at the scale they need. The Cell Shuttle is an automated and closed end-to-end manufacturing solution that is flexible and scalable, enabling customers to run exact processes specified for their cell therapy. Compared with the current manual manufacturing processes for cell therapy, the Cell Shuttle’s next-generation automated manufacturing solution has 10 times the scalability (meaning 10 times more patient doses can be produced simultaneously), enables a three-fold reduction in process failure rates and will reduce the per-patient manufacturing cost by up to 70 percent for most processes.
