Full stack Lead software Engineer

Website Danaher

Full stack Lead software Engineer

Beckman Coulter Diagnostics  

Bangalore, Karnātaka, India 
Category  Digital Products Development 
Job IdR1312277
Location  Bangalore, Karnātaka, India

The Lead software Engineer for Beckman Coulter Diagnostics is responsible to architect, design, Code, debug and implement software features, enhancements working collaboratively with team. He or She will develop quick prototypes to demonstrate the design concepts and product ideas to team and management. Furthermore, the candidate will work independently as well as with SME’s

 

This position reports to the Software Engineering manager of Clinical informatics product and is part of the Digital Solutions R&D group located in Bengaluru and will be an on-site role.

 

In this role, you will have the opportunity to:

  • Architect, design, code, and test robust software solutions while ensuring compliance with regulatory standards.
  • Investigate/Understand complex issues coming in from the field and drive to root cause
  • Champion software development best practices to maintain high-quality standards.
  • Develop prototypes to demonstrate design concepts, collaborating effectively with cross-functional teams to translate needs into actionable features.

 

The essential requirements of the job include:

  • Bachelor’s/Master’s degree in Computer Science, Computer Engineering, or a related field with 7+ years proven experience in C# .Net Programming.
  • At least 2 years of experience in front-end web development using modern frameworks such as AngularJS, React, and TypeScript.
  • At least 2 years of experience with scripting languages such as Python or Shell.
  • Hands on experience on DevOps, Continuous Integration, delivery and deployment, version Control (e.g., git).

It would be a plus if you also possess previous experience in:

  • Experience in medical device design & development in Agile environment is a plus.
  • Experience in cloud applications AWS/Azure.
  • Understanding of software development processes for a regulated environment (FDA/ISO13485) and experience in medical device verification is a plus

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