Client System Manager

ACG World; Mumbai; On-site; INR 3,500,000 - 6,500,000; Full time

Job summary

ACG World is seeking an experienced Edge Software Manager to lead a cross‑functional team focused on L2 pharma manufacturing software. You will drive architecture, modernization of legacy systems, and real‑time performance improvements in a hands‑on leadership role.

You will supervise .NET Core / C++ development, RESTful APIs, CUDA optimization, and secure CI/CD while ensuring GMP/21 CFR Part 11 compliance and strong teamwork across QA, DevOps, and PLC/hardware groups.

Qualifications

• Over 10 years of software development experience.
• Strong proficiency in .NET Core / .NET 6+ and C# with modern patterns.
• Solid C++ experience (11/14/17/20) and OOP design.
• Hands-on CUDA programming for GPU-accelerated tasks.

Responsibilities

• Lead cross‑functional team of .NET and C++ developers for L2 pharma systems.
• Plan sprints, conduct code reviews, and ensure quality and deadlines.
• Architect and modernize backend modules, APIs, and CI/CD pipelines.
• Coordinate with PLC/hardware teams for seamless integration.
• Mentor engineers and uphold regulatory compliance and documentation.

Skills

Dotnet/C#

C++

CUDA

REST APIs

Embedded systems

Agile/Scrum

Team leadership

Performance profiling

Docker

Git

Education

B.E./B.Tech in Computer Science or Electronics

M.Tech / MBA with Technology background

Tools

Docker

Git

ASP.NET Core

Job description

We are seeking an experienced Edge Software Manager with a strong background in .NET/C# application development and C++ programming to lead our software team in building and managing Level 2 (L2) supervisory control and data systems for pharmaceutical manufacturing operations. This is a hands‑on leadership role that combines deep technical expertise with team management skills to deliver high‑quality, compliant, and high‑performance software solutions.

The role bridges enterprise .NET application development and real‑time/embedded C++ systems, ensuring seamless integration between L2 software layers, PLC/hardware interfaces, and manufacturing execution systems (MES). The incumbent will oversee the full development lifecycle - from architecture design and modernization of legacy systems to performance optimization and cross‑team collaboration.

C. Primary Responsibilities

• Lead and manage a cross‑functional team of .NET and C++ developers focused on L2 pharma manufacturing systems.
• Mentor junior and mid‑level developers, foster a culture of technical excellence and collaboration.
• Conduct code reviews, enforce coding standards, and uphold software quality best practices.
• Plan sprints, assign tasks, and track delivery in agile/scrum workflows.
• Oversee design, development, and modernization of backend modules using .NET Core / .NET 6+.
• Architect and build RESTful APIs using ASP.NET Core Web API following SOLID and clean architecture principles.
• Drive migration of legacy WPF/WCF/.NET Framework systems to scalable, secure REST‑based architectures.
• Support Docker‑based containerization and cloud/on‑premise deployments.
• Ensure implementation of unit testing (xUnit / NUnit / MSTest) and CI/CD pipelines.
• Leverage AI‑assisted development tools (e.g., GitHub Copilot) responsibly.

3. C++ / CUDA / Embedded Systems

• Lead development and optimization of C++ components for high‑performance and real‑time applications.
• Drive CUDA programming for GPU‑based parallel computing tasks relevant to manufacturing data processing.
• Oversee software integration with embedded systems, PLCs, and hardware interfaces on Linux‑based platforms.
• Ensure performance profiling and optimization of GPU‑accelerated and multi‑threaded applications.
• Collaborate with PLC/C++ hardware teams for seamless machine communication integration.
• Design and govern the software architecture for L2 supervisory systems in pharma manufacturing.
• Ensure seamless data exchange between L2 software, MES, SCADA, and L1 device layers.
• Define integration protocols and APIs for device communication and data acquisition.
• Oversee performance, reliability, and security of manufacturing software systems.

5. Quality, Compliance & Documentation

• Ensure all software development aligns with pharma industry regulatory requirements (GMP, 21 CFR Part 11, etc.).
• Maintain comprehensive technical documentation for architecture, APIs, and integration interfaces.
• Support validation activities (IQ/OQ/PQ) for manufacturing software systems.

D. Key Result Areas

• On‑time delivery of L2 software modules and modernized backend services.
• High‑quality, unit‑tested, and well‑documented codebase.
• Smooth integration between .NET applications and C++/hardware layers.
• Improved system performance through CUDA/GPU optimization and profiling.
• Regulatory compliance of all delivered software in pharma manufacturing context.
• Team capability growth through active mentoring and technical leadership.

E. Required Skills & Experience

Core Technical Skills

• 10+ years of relevant software development experience.
• Strong proficiency in .NET Core / .NET 6+ and C# including modern features, design patterns, and clean architecture.
• Solid experience in C++ (11/14/17/20) including modern C++ features and OOP design principles.
• Hands‑on experience with CUDA programming for GPU‑based parallel computing.
• Experience in device integration using C++ with embedded systems and hardware interfaces.
• Proficiency in developing RESTful APIs using ASP.NET Core Web API.
• Familiarity with performance profiling and optimization, particularly for GPU‑accelerated applications.
• Proficiency in debugging multi‑threaded environments.
• Experience with containerization technologies such as Docker.
• Experience with version control systems (Git).

Leadership & Soft Skills

• Proven ability to lead a team of engineers with strong communication and mentoring skills.
• Solid understanding of software architecture and design principles.
• Experience working in agile/scrum development environments.
• Strong problem‑solving skills with an analytical mindset.
• Ability to collaborate across cross‑functional teams (QA, DevOps, Product, PLC/Hardware).

F. Preferred Qualifications

• Prior experience in pharma manufacturing systems (L2/MES/SCADA).
• Knowledge of regulatory frameworks: GMP, 21 CFR Part 11, GAMP 5.
• Familiarity with frontend technologies such as React.js.
• Experience with OpenCL or other GPU computing frameworks.
• Knowledge of Python for scripting and data processing.
• Experience with embedded systems or hardware programming beyond standard C++ integration.
• Exposure to cloud platforms (Azure) for hybrid manufacturing deployments.

G. Educational Requirements

Level of Education

B.E. / B.Tech in Computer Science, Electronics, or related field

M.Tech / MBA with Technology background

Experience

10+ years in software development with .NET and C++ exposure

Prior experience in pharma / industrial manufacturing software systems