**What you will do:**

+ Design, develop, and maintain complex **C++/Python applications** for Linux and Windows systems in a regulated medical device environment.
+ Define robust **software architecture and system design** (including UML-based modeling) and provide well-founded development effort estimations.
+ Implement, extend, and integrate **software modules and system interfaces** , ensuring scalable and high-quality solutions.
+ Document development work in accordance with **software engineering best practices** , ensuring traceability and compliance readiness.
+ Plan, execute, and document **verification and validation (V&V;)** activities with a strong focus on quality assurance.
+ Collaborate cross-functionally and coordinate work packages to ensure smooth execution across teams and stakeholders.
+ Lead, mentor, and support team members, contributing to **continuous improvement of development processes** .
+ Contribute to software infrastructure and **DevOps initiatives** , including defining scalable Git repository structures and coordinating code migration.
+ Drive **build system modernization** , including migration from QBS to CMake-based environments.
+ Design and implement **Docker-based development and build environments** .
+ Set up, run, and optimize **CI/CD pipelines** using Jenkins and GitLab, including supporting migration to GitLab pipelines.

**Required Qualifications:**

+ Bachelor’s degree in Computer Science, Software Engineering, Technical Informatics, or a related field.
+ **Minimum 5+ years of hands-on experience** in software development.
+ Strong programming expertise in **C++ and Python** , with experience building applications for **Linux and Windows environments** .
+ Strong proficiency in **object-oriented design, software architecture, and system design** .




+ Proven ability to **understand business/technical requirements and translate them into structured deliverables and implementation plans** .
+ Experience designing, documenting, and implementing scalable software systems.
+ Hands-on experience with **build systems (CMake)** and **migration from legacy environments such as QBS** .
+ Working knowledge of **C#** and multi-language development environments.
+ Familiarity with **DevOps practices** including CI/CD pipelines, Docker, and version control systems (Git).
+ Experience working in an **Agile development environment** with sprint-based delivery models.
+ **Strong communication skills** with the ability to collaborate effectively across cross-functional teams.
+ **Understanding of AI tools and modern development productivity tools** (e.g., AI-assisted coding, testing, debugging).

**Preferred Qualifications:**

+ Experience working in a **regulated or medical device software workplace** .
+ Knowledge of **software development lifecycle (SDLC)** , verification & validation processes, and compliance standards.
+ Experience with **CI/CD tools** such as Jenkins and GitLab pipelines.
+ Strong collaboration, communication, and **technical leadership capabilities** .

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.
Stryker Corporation is an equal opportunity employer.

Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status.

Stryker is an EO employer – M/F/Veteran/Disability.

Required Skill Profession

Other General

📌 Senior Software Engineer (Gurugram)
🏢 Stryker
📍 Gurugram