Eng II, Software Job at Baxter (Bengaluru)

New

Eng II, Software

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

A Bachelor's or Master's degree in Computer Science, Software Engineering, or a related field is required
Must have a minimum of 4-7 years of proven experience in web development
Hands-on experience in creating solutions in PAAS environment on MS AZURE (preferred) / AWS/ Google Cloud environments
Programming Languages: C#, Javascript
Hands-on experience in .NET Framework and .NET Core
Good understanding of database technologies including Azure SQL DB / MS SQL
Working knowledge on Windows/Linux Server/Backend Components
Enterprise Integration: Design patterns for enterprise integration REST and Microservices
Familiarity with API development using SOAP is a plus
Familiarity with Development & Continuous Integration tools such as Azure DevOps

Job Responsibility

Directly responsible for implementing SW modules/subsystems of cloud-based Web Applications and solutions to contribute towards new product development programs, sustenance activities and field issue resolution efforts
Effectively collaborate with cross-functional teams, including architects, developers, QA, and other stakeholders, to understand the SW requirements
Directly responsible for understanding and implementing architectural patterns and design techniques to translate requirements into modular, scalable software and Web solutions, that meet user needs
Collaborate with architect and developers to apply principles of SDLC and methodologies/processes such as IEC 62304, Lean, Agile, CI to deliver and maintain design outputs including code and documentation that meet applicable statutory and regulatory requirements
Directly responsible for debugging and testing of SW modules to ensure defect free operation and provide input in code quality, security reviews to meet industry-wide quality & security standards
Embrace agility and adapt to changes in the project requirements and priorities and deliver high quality and timely deliverables
Attend sprint planning, daily standups, demos, retrospectives and software design meetings
Follow documented procedures for all activities related to the Bardy Dx Quality System
Complete other duties as assigned

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Eng II, Systems

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 6 yrs of experience, mainly in System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Demonstrated experience in accomplishing objectives
Able to deliver on multiple projects simultaneously
Self-motivated with good interpersonal skills

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, Design trade-offs and Risk assessment early in the development cycle working independently or under the guidance of senior staff
Provide your technical expertise to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Excels in the development of Use Case for product or solution based on intimate knowledge of customers and their environments
Use tools such as DOORS, POLARION or equivalent and excels in the management of requirements and decomposition of system level requirements to modules
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Identify development issues and facilitates in the resolution using optimal technology solutions
Supports in the Usability Engineering activities to ensure the application of human factor in the development of products or solutions to demonstrate compliance to IEC 62366 and FDA guidance
Completes detailed, high quality technical documentation to capture and communicate designs
Support integration issues during development tests and ensure module / system development is successful
Actively collaborate with software and hardware engineers to aid in the design development

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

New

Eng II, Systems C&S

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Electronics Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
3 to 8 yrs of experience, mainly in Codes and Standards, testing & System engineering function of Electro-Mechanical System Design
Experience in Medical Device development, FDA Regulations and MDR
Exposure to Usability Engineering Process
Experience in QFD, Pugh Matrix, CTQ, DFR, DFX
Strong interpersonal skills with the ability to collaborate with others in a team environment
Understanding of and adherence to FDA, ISO and IEC design control procedures, regulations and standards
Excellence in Medical Devices safety (IEC 60601-1 and collaterals for medical devices like cardiology, patient monitoring and respiratory therapies), FDA Regulations or other applicable regulatory requirements
Excellence in Medical Device software life cycle processes (IEC 62304), EMI/ EMC requirements, REACH, ROHS and Biocompatibility
Demonstrated experience in accomplishing objectives

Job Responsibility

Identify and define internal and external customer needs, functions, performance, usability and safety requirement for product or solution with thorough knowledge and understanding constraints - Business and Regulatory, C&S assessment early in the development cycle working independently or under the guidance of senior staff
Execute compliance testing as a part of the development team to ensure that the project successfully meets cost, quality and schedule targets throughout the product life cycle
Use tools such as DOORS and excels in the management of requirements and decomposition of system level requirements to modules and their respective compliance requirements
Carry out risk management process in accordance with the EN ISO 14971 throughout product life cycle to ensure compliance and product safety
Excels in the application of principles of Reliability and Robustness in the development of products or solution
Completes detailed, high quality technical documentation to capture and communicate designs
As Lead integrator for the product proactively look out for integration issues during development tests and ensure module / system development is successful
Lead the effort in complying with IEC 60601-1 and collateral standards to obtain product approvals from external safety test labs and notified bodies (DQS, UL, ETL, TUV, LNE, etc.)
Excels in obtaining and maintaining 3rd party Product Certifications, Type approvals and technical files
Actively engage with verification and validation engineers to aid in the development of verification scripts with good test coverage

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Eng II, Test

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelors / master’s in computer science, Computer Engineering, Software Engineering or related field and 4+ years of related experience
Minimum 4+ years of Automation or development background
Working experience in DevOps, CI/CD pipeline methodology
Experience with a variety of types of testing, including regression, performance, stress, unit, integration, and security testing using automation framework
Technical expertise in automated UI UX workflow using Squish
Expertise in Robot Framework, Python, Squish, and Shell scripting
Hands-on experience on Git, HP-ALM tool and Polarion is an added advantage
Hands-on experience on creating automation framework, and functional level software automation test scripts and test execution dashboards
Knowledge of medical device software development is highly preferred including knowledge of standards such as IEC 62304, ISO 14971

Job Responsibility

Participate in PI planning and daily SCRUM meetings and ensure stories/tasks are updated in JIRA every day
Complete all the Q&R training needed before time
Analyze subsystem & system requirements with guidance from lead and other seniors
Design tests covering the system / subsystem requirements – following robust test design techniques covering all positive and negative scenarios
Ensure test designs in the identified test tool [HP ALM] with the needed traceability
Use JIRA as work management and bug management tool
Set up and create the required test infrastructure [software, hardware] following the lab guidelines strictly
Maintain automation framework, and write
Execute the tests as per the design
Collaborate with development teams to confirm defects

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Eng II, V&V

As System Verification Test engineer for Infusion pumps team within Medication d...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
Overall 5 to 8 yrs of experience with minimum 2 years in System Verification testing and performance testing
Hands on experience in overall final design verification/validation(V&V) testing of medical products
Relevant technical testing/reliability experience in electro-mechanical, electrical testing of Medical Devices
An understanding of test methods and processes as well as the methods used to verify product in the realms of
mechanical, electrical, functional testing environments
Basic hands on experience in data analysis of Performance testing and Sample size calculations for variable/Attribute data
Experience in Tools like Minitab( Data Analysis) / JIRA ( Defect ) / ALM ( test Environment) etc.
Understanding of hardware and software product design methodologies and test practices
Experience in medical device or similar product development, design verification/validation, system integration (hardware/Subsystem/Software), risk management, reliability engineering, process validation and Quality systems

Job Responsibility

Lead/Execute, perform, summarize and report out verification test activities Medical devices
Understand URS (User requirements) / System Requirements and prepare the System Level Test cases and Prepare test procedures
Understand the product functionality and perform the Functional and Performance testing for the product
Lead/Support and perform all Design Verification activites
Perform Installation/Operational/Performance Qualification Protocols
Prepare Traceability Matrices and Final Reports
Support compliance/ closure of Regulatory and Quality requirements
Follow Test instructions and Test protocols
Follow instructions clearly from Design engineers during Test execution
Support Design engineers in Test fixture creation, building up & tearing down Test equipment

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Eng II, V&V

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
Overall 5 to 8 yrs of experience with minimum 2 years in System Verification testing and performance testing
Hands on experience in overall final design verification/validation(V&V) testing of medical products
Relevant technical testing/reliability experience in electro-mechanical, electrical testing of Medical Devices
An understanding of test methods and processes as well as the methods used to verify product in the realms of
mechanical, electrical, functional testing environments
Basic hands on experience in data analysis of Performance testing and Sample size calculations for variable/Attribute data
Experience in Tools like Minitab( Data Analysis) / JIRA ( Defect ) / ALM ( test Environment) etc.
Understanding of hardware and software product design methodologies and test practices
Experience in medical device or similar product development, design verification/validation, system integration (hardware/Subsystem/Software), risk management, reliability engineering, process validation and Quality systems

Job Responsibility

Lead/Execute, perform, summarize and report out verification test activities Medical devices: Which includes but not limited to: Understand URS (User requirements) / System Requirements and prepare the System Level Test cases and Prepare test procedures
Understand the product functionality and perform the Functional and Performance testing for the product
Lead/Support and perform all Design Verification activites
Perform Installation/Operational/Performance Qualification Protocols
Prepare Traceability Matrices and Final Reports
Support compliance/ closure of Regulatory and Quality requirements
Follow Test instructions and Test protocols
Follow instructions clearly from Design engineers during Test execution
Support Design engineers in Test fixture creation, building up & tearing down Test equipment
Support Lab logistics and maintain the material supply for testing requirements

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Eng II, V&V

As System Verification Test engineer for Infusion pumps team within Medication d...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
Overall 5 to 8 yrs of experience with minimum 2 years in System Verification testing and performance testing
Hands on experience in overall final design verification/validation(V&V) testing of medical products
Relevant technical testing/reliability experience in electro-mechanical, electrical testing of Medical Devices
An understanding of test methods and processes as well as the methods used to verify product in the realms of
mechanical, electrical, functional testing environments
Basic hands on experience in data analysis of Performance testing and Sample size calculations for variable/Attribute data
Experience in Tools like Minitab( Data Analysis) / JIRA ( Defect ) / ALM ( test Environment) etc.
Understanding of hardware and software product design methodologies and test practices
Experience in medical device or similar product development, design verification/validation, system integration (hardware/Subsystem/Software), risk management, reliability engineering, process validation and Quality systems

Job Responsibility

Lead/Execute, perform, summarize and report out verification test activities Medical devices
Understand URS (User requirements) / System Requirements and prepare the System Level Test cases and Prepare test procedures
Understand the product functionality and perform the Functional and Performance testing for the product
Lead/Support and perform all Design Verification activites
Perform Installation/Operational/Performance Qualification Protocols
Prepare Traceability Matrices and Final Reports
Support compliance/ closure of Regulatory and Quality requirements
Follow Test instructions and Test protocols
Follow instructions clearly from Design engineers during Test execution
Support Design engineers in Test fixture creation, building up & tearing down Test equipment

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Eng II, System Verification

This is where your work makes a difference. At Baxter, we believe every person—r...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Bachelor's Degree in Mechanical engineering, Electrical Engineering, Software Engineering, Computer Science, Bio-Medical, Industrial Engineering or related field
Overall 5 to 8 yrs of experience with minimum 2 years in System Verification testing and performance testing
Hands on experience in overall final design verification/validation(V&V) testing of medical products
Relevant technical testing/reliability experience in electro-mechanical, electrical testing of Medical Devices
An understanding of test methods and processes as well as the methods used to verify product in the realms of
mechanical, electrical, functional testing environments
Basic hands on experience in data analysis of Performance testing and Sample size calculations for variable/Attribute data
Experience in Tools like Minitab( Data Analysis) / JIRA ( Defect ) / ALM ( test Environment) etc
Understanding of hardware and software product design methodologies and test practices
Experience in medical device or similar product development, design verification/validation, system integration (hardware/Subsystem/Software), risk management, reliability engineering, process validation and Quality systems

Job Responsibility

Lead/Execute, perform, summarize and report out verification test activities Medical devices: Which includes but not limited to:
Understand URS (User requirements) / System Requirements and prepare the System Level Test cases and Prepare test procedures
Understand the product functionality and perform the Functional and Performance testing for the product
Lead/Support and perform all Design Verification activites
Perform Installation/Operational/Performance Qualification Protocols
Prepare Traceability Matrices and Final Reports
Support compliance/ closure of Regulatory and Quality requirements
Follow Test instructions and Test protocols
Follow instructions clearly from Design engineers during Test execution
Support Design engineers in Test fixture creation, building up & tearing down Test equipment

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

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