Full Stack Senior Software Engineer

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology

You will thrive in a culture of belonging where your unique viewpoint matter. And by harnessing a system of continuous improvement, you help turn ideas into impact innovating at the speed of life.

As a Senior Software Engineer, you will be responsible to Architect, Design, Code, Debug and Implement software features and enhancements working collaboratively with the team. You 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 SMEs.

This position reports to the Senior Software Engineering manager of Digital solution Cloud platform and is part of the Digital Solutions RD group on site.

In this role, you will have the opportunity to:

• Understand the overall requirements of the product/platform and specifically for the assigned feature/module.
• Design and Develop code as per the software requirements and generate Unit Test cases, Investigate software / system problems and fix defects and track it to closure
• Collaborate with cross-functional teams (locally globally) to ensure product releases meet quality, performance, scalability, reliability and schedule goals.

The essential requirements of the job include:

• Bachelor’s/Master’s degree in Computer Science, Computer Engineering, or a related field with 5+ years proven experience in Java/J2EE/.Net Programming.
• At least 2 years of experience in front-end web development using modern frameworks such as AngularJS or React on Azure Cloud and working with Gen AI based product development
• Hands on experience on Java Script, Rest API, Microservice Architecture, 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.
• Understanding of software development processes for a regulated environment (FDA/ISO13485) and experience in medical device verification is a plus

Disclaimer : This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.