Software Developer

Clario

Bengaluru

Remote

INR 900,000 - 1,500,000

Full time

6 days ago
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Benefits offered by this job

Competitive pay & incentives
Provident fund & medical insurance
Remote work flexibility

Job summary

Clario, part of Thermo Fisher Scientific, Bengaluru, is seeking a Software Developer to design, develop, validate, and support software solutions for Digital Patient products. You will work in a regulated environment, collaborating with cross-functional teams to ensure quality, reliability, and compliance in clinical trial software.

The role emphasizes .NET/C# development, SQL data handling, and maintaining validated states through change control, with remote-friendly work options and growth

Qualifications

  • Bachelor's degree in CS or related field.
  • Minimum 2 years of software development experience.
  • Strong C# and SQL experience in the .NET ecosystem.
  • Experience in validated/regulatory software environments is a plus.

Responsibilities

  • Design, develop, maintain, and support software applications for Digital Patient products.
  • Participate in architecture, technical design, and development planning throughout the product lifecycle.
  • Create validation documentation and maintain products in a validated state through change control processes.
  • Develop requirements, technical designs, and test environments aligned with project timelines and quality standards.
  • Troubleshoot, investigate, and resolve application and system issues.
  • Collaborate with cross-functional teams to deliver value and improve customer outcomes.

Skills

C#
SQL
.NET
OO programming
English

Education

Bachelor's degree in CS/related

Tools

SQL Server
Visual Studio

Job description

Join Clario, a part of Thermo Fisher Scientific and help build the technology that powers patient-focused clinical trials around the world. As a Software Developer within our Digital Patient business, you will contribute to the design, development, validation, and support of software solutions that enable the collection and management of critical clinical research data. Working within a regulated environment, you will collaborate with cross-functional teams to develop innovative products, enhance system capabilities, and maintain the high standards of quality, reliability, and compliance required for clinical trial technology.

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.

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