Principal Manufacturing Software Engineer

DHR Holding India; Bengaluru; On-site; INR 3,500,000 - 5,500,000; Full time

Job summary

DHR Holding India seeks a Principal Manufacturing Software Engineer to lead the development of software platforms for diagnostic instruments in a regulated medical device setting. You will build C#/C++ applications interfacing with hardware, manage electronic Device History Records, and enable AI-driven quality and process optimization on site in Bangalore.

You will collaborate with R&D, Manufacturing, and Quality to ensure compliant production data handling and robust test and calibration

Qualifications

• 18 years of software development experience or 8+ years with a Master’s degree.
• Expert-level proficiency in C#/C++ and other OO languages; strong WPF knowledge.
• Experience interfacing with hardware and test equipment; regulated environments.
• Solid SQL data design and production data management; cloud development with AWS Lambda.

Responsibilities

• Architect, design, and lead development of scalable manufacturing software for instruments.
• Develop C#/C++ applications interfacing with hardware and automating test/calibration.
• Build systems to collect/store/retrieve eDHR manufacturing data securely and compliantly.
• Collaborate with R&D, Manufacturing, and Quality to ensure software validation.
• Leverage manufacturing data to create AI tools for failure prediction and calibration optimization.

Skills

C#/C++

WPF

TCP/IP

CAN/UDP

Java

Python

SQL

Education

Bachelor's degree in CS/Engineering

Master's degree in CS/Engineering

Tools

AWS Lambda

Job description

Job Summary

The Principal Manufacturing Software Engineer is responsible for Leading development of manufacturing software platforms for diagnostic instruments, including testing, calibration, firmware flashing, and validation. Build C#/C++ applications that interface with hardware, manage compliant production data (electronic Device History Record), and enable AI-driven quality and process optimization. Collaborate across R&D, Manufacturing, and Quality functions in a regulated medical device environment.

This position reports to the Principal Software/Firmware Engineer and is part of the Software/Firmware Engineering job family located in Bangalore, India and will be an on-site role.

Responsibilities

• Architect, design, and lead the development of a scalable and robust software platform for instrument manufacturing. This includes software for production line testing, component calibration, firmware flashing, and support SQA to do manufacturing software verification.


• Develop sophisticated software applications (primarily in C#/C++) that interface directly with our diagnostic instruments and test fixtures to automate complex test sequences and calibration procedures.


• Design and implement the systems for collecting, storing, and retrieving all manufacturing data for each instruments electronic Device History Record (eDHR). Ensure all data is secure and compliant with regulatory requirements.


• Work intimately with R&D hardware and firmware engineers to understand instrument test requirements, with Manufacturing Engineers to optimize production workflows, and with Quality Assurance to ensure software validation.


• Utilize past manufacturing data to develop AI tools to predict the modules/instruments failure and optimize the calibration process

Essential Requirements

• Minimum 18 years of software development experience with a Bachelor s or 8+ years of experience with Master s degree in Computer Science, Computer Engineering, or a related field


• Expert-level proficiency in an object-oriented language such as C#/C++ , Java, Python.Deep knowledge of WPF, strong development experience in TCP/IP, CAN, UDP and other network interfaces.


• Proven experience designing software that interfaces with and controls physical hardware and test equipment.


• Strong experience with database design (SQL) and data management for production environments and strong experience in Cloud program development, AWS Lambda APIs.


• Experience working in a regulated industry such as diagnostic/ medical devices, aerospace, or automotive.

Travel, Motor Vehicle Record & Physical/Environment Requirements

• Ability to travel as required and collaborate with global internal and external stakeholders.

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

• Direct experience developing software under a diagnostic/ medical device quality management system (ISO 13485)


• Familiarity with the requirements for software validation in an FDA-regulated environment

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.