Scada Ignition Engineer

Stryker; Gurugram District; On-site; INR 1,200,000 - 2,200,000; Full time

Job summary

Stryker is seeking a software engineering professional to assist with prototyping, bench testing, and research to support medical device product design. You will draft and review design documents, interpret user needs, and ensure compliance with regulatory requirements.

Under supervision you will design, develop, modify, evaluate, and verify software components, participate in code reviews, and collaborate with cross-functional teams to ensure project success and gain valuable experience.

Qualifications

• Bachelor's degree in Software Engineering/CS or related field, with 3+ years of work experience.
• Good experience working on Scada ignorance.
• Exposure to programming skills.
• Experience with integrated development environments (IDE) for projects.
• Experience with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software.
• Integration and deployment processes.
• Software Development Life Cycle processes.
• Application Lifecycle Management /Traceability tools.
• Regulatory and compliance standards applied to the SDLC.

Responsibilities

• Assist with prototyping and bench testing.
• Support problem solving, identify potential solutions, and evaluate them against requirements.
• Under supervision, conduct research and studies to support product design.
• Code development time/resource estimation to support projects.
• Generate and review the necessary documents with project teams (requirements/design/architecture/bugs/test).
• Interpret customer needs and understands design inputs.
• Understand the product’s intended use and clinical procedures.
• Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements.
• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures.
• Learn R&D procedures like design controls and risk management, per the Quality Management System.
• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member.
• Learn procedures, policies, processes, systems, and technology required.
• Work on problems in limited scope; purposefully learn while gaining experience.
• Design, develop, modify, evaluate and verify software components for medical devices.
• In code reviews apply design principals, coding standards and best practices

Skills

Programming exposure

IDE experience

Static analysis

Dynamic analysis

Memory management

Code coverage

SDLC processes

ALM/Traceability

Regulatory standards

Education

Bachelor's degree in CS/Software Eng

Tools

IDE

Static analysis

Dynamic analysis

Job description

• Assist with prototyping and bench testing
• Support problem solving, identify potential solutions, and evaluate them against requirements
• Under supervision, conduct research and studies to support product design
• Generate and review the necessary documents with project teams (requirements/design/architecture/bugs/test)
• Interpret customer needs and understands design inputs
• Understand the product’s intended use and clinical procedures
• Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements
• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures
• Learn R&D procedures like design controls and risk management, per the Quality Management System
• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member
• Learn procedures, policies, processes, systems, and technology required
• Work on problems in limited scope; purposefully learn while gaining experience
• Design, develop, modify, evaluate and verify software components for medical devices
• In code reviews apply design principals, coding standards and best practices

What you will do:

• Assist with prototyping and bench testing
• Support problem solving, identify potential solutions, and evaluate them against requirements
• Under supervision, conduct research and studies to support product design
• Code development time/resource estimation to support projects
• Generate and review the necessary documents with project teams (requirements/design/architecture/bugs/test)
• Interpret customer needs and understands design inputs
• Understand the product’s intended use and clinical procedures
• Understand fundamental industry standards, design requirements and test strategies which align with regulatory requirements
• With supervision, create or refine engineering documentation, such as the Design History file per company design control procedures
• Learn R&D procedures like design controls and risk management, per the Quality Management System
• Work cooperatively with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing and Project Management to ensure project success and contribute to the project as a team member
• Learn procedures, policies, processes, systems, and technology required
• Work on problems in limited scope; purposefully learn while gaining experience
• Design, develop, modify, evaluate and verify software components for medical devices
• In code reviews apply design principals, coding standards and best practices

What you will need:

Minimum Qualifications (Required):

Bachelor's degree in Software Engineering/ Computer Science or related discipline with 3+ years of work experience

Good experience working on Scada ignorance

Preferred Qualifications (Strongly desired):

• Exposure to programming skills
• Experience with integrated development environments (IDE) for projects
• Experience with tools for static/dynamic analysis, memory management, code coverage and techniques for analyzing software
• Integration and deployment processes
• Software Development Life Cycle processes
• Application Lifecycle Management /Traceability tools
• Regulatory and compliance standards applied to the SDLC (Software Development Life Cycle)

Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.