Software Developer

US Biomedical Systems India Pvt Ltd.; Bengaluru; Hybrid; INR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Competitive pay

Provident fund

Medical insurance

Remote work flexibility

Job summary

Clario seeks a software engineer to design, develop, and support Digital Patient product software within a regulated environment. You will participate in architecture, validation, and lifecycle activities, ensuring quality and timely delivery across cross-functional teams.

The role requires a strong foundation in C#/.NET, SQL, and SDLC principles, along with hands-on programming experience and a collaborative mindset. Hybrid work options and ongoing professional development are offered.

Qualifications

• Bachelor's degree in Computer Science, Software Engineering, Information Technology, or related technical discipline, or equivalent professional experience.
• Minimum 2 years of experience in a commercial software development environment.
• Strong experience developing applications within the Microsoft .NET ecosystem.
• Hands-on programming experience using C# and object-oriented development principles.
• Experience working with SQL and relational database technologies.
• Understanding of software development lifecycle methodologies, software design principles, and testing practices.
• Experience developing, maintaining, and supporting business-critical software applications.
• Exposure to software validation, regulated environments, or quality-controlled development processes is advantageous.

Responsibilities

• Design, develop, maintain, and support software applications for Digital Patient products and services.
• Participate in software architecture, technical design, and development planning activities throughout the product lifecycle.
• Contribute to product configuration, implementation, and maintenance activities, including the creation of validation documentation.
• Develop requirements specifications, technical designs, software components, and test environments in accordance with project timelines and quality standards.
• Support software validation activities and ensure products remain in a validated state throughout change control processes.
• Troubleshoot, investigate, and resolve application, system, and technical support incidents.
• Collaborate with cross-functional stakeholders to develop innovative solutions that enhance product value and improve customer outcomes.
• Provide feedback on project timelines, technical risks, dependencies, and delivery plans.
• Participate in code reviews, testing activities, quality assurance efforts, and continuous improvement initiatives.
• Contribute to enhancements in software development processes, tools, and operational practices.
• Ensure compliance with applicable quality standards, regulatory requirements, and company procedures.
• Maintain knowledge of relevant SOPs, software development methodologies, and industry best practices.
• Support regulatory compliance requirements, including those associated with healthcare and regulated software development environments.
• Continuously develop technical skills and participate in training activities to support personal and professional growth.

Skills

C#

Microsoft .NET

SQL

Education

Bachelor's degree in Computer Science / Software Engineering / IT

Job description

What We Offer

• Competitive pay and incentives.
• Provident fund and medical insurance.
• Engaging employee programs and local events.
• Modern office spaces and remote work flexibility.

What You'll Be Doing

• Design, develop, maintain, and support software applications for Digital Patient products and services.
• Participate in software architecture, technical design, and development planning activities throughout the product lifecycle.
• Contribute to product configuration, implementation, and maintenance activities, including the creation of validation documentation.
• Develop requirements specifications, technical designs, software components, and test environments in accordance with project timelines and quality standards.
• Support software validation activities and ensure products remain in a validated state throughout change control processes.
• Troubleshoot, investigate, and resolve application, system, and technical support incidents.
• Collaborate with cross-functional stakeholders to develop innovative solutions that enhance product value and improve customer outcomes.
• Provide feedback on project timelines, technical risks, dependencies, and delivery plans.
• Participate in code reviews, testing activities, quality assurance efforts, and continuous improvement initiatives.
• Contribute to enhancements in software development processes, tools, and operational practices.
• Ensure compliance with applicable quality standards, regulatory requirements, and company procedures.
• Maintain knowledge of relevant Standard Operating Procedures (SOPs), software development methodologies, and industry best practices.
• Support regulatory compliance requirements, including those associated with healthcare and regulated software development environments.
• Continuously develop technical skills and participate in training activities to support personal and professional growth.

What We Look For

• Bachelor's degree in Computer Science, Software Engineering, Information Technology, or a related technical discipline, or equivalent professional experience.
• Minimum 2 years of experience in a commercial software development environment.
• Strong experience developing applications within the Microsoft .NET ecosystem.
• Hands-on programming experience using C# and object-oriented development principles.
• Experience working with SQL and relational database technologies.
• Understanding of software development lifecycle methodologies, software design principles, and testing practices.
• Experience developing, maintaining, and supporting business-critical software applications.
• Exposure to software validation, regulated environments, or quality-controlled development processes is advantageous.
• Mobile application development experience is desirable.
• Strong analytical and problem-solving skills with the ability to troubleshoot technical issues effectively.
• Excellent organizational and communication skills with the ability to work collaboratively across teams.
• Ability to manage multiple priorities and adapt to changing project requirements.
• Self-motivated approach with a commitment to continuous improvement and professional development.
• Professional fluency in English.

At Clario, a part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence. It's a cause that unites and inspires us. It's why we come to work and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.