Sr. Software Engineer

Role Overview: At Clario, a part of Thermo Fisher Scientific, you will be a Software Engineer responsible for designing, developing, testing, and maintaining software applications used in regulated clinical trial environments. You will work closely with cross-functional stakeholders to deliver high-quality, compliant solutions. Key Responsibilities: - Analyze, design, develop, test, debug, and maintain software enhancements and new applications using C#, .NET, and SQL - Perform requirements analysis and proactively identify gaps, ambiguities, and risks - Clearly distinguish business requirements from technical design and implementation - Follow established development patterns, coding standards, and software lifecycle processes - Write clear, maintainable code with appropriate unit test coverage - Identify, document, and communicate software defects, including steps to reproduce and workarounds - Conduct code and design reviews to identify weaknesses, alternatives, and trade-offs - Deliver high-quality, tested code on schedule with a low defect rate - Demonstrate application features and fixes to product management and end users - Partner with Quality Assurance by advising on regression testing focus areas - Troubleshoot production and support issues, isolating defects to specific components - Estimate development effort based on detailed design and contribute to planning activities - Adhere to organizational Standard Operating Procedures (SOPs) and regulatory requirements Qualifications Required: - Bachelors degree strongly preferred - 3+ years of professional software development experience - Strong hands-on experience with C#, .NET, and basic SQL - Experience in clinical trials, life sciences, or pharmaceutical environments preferred - Working knowledge of drug development processes and regulatory requirements, including GxP and 21 CFR Part 11 - Proven analytical and problem-solving skills - Ability to work effectively both independently and in a team environment - Strong written and verbal communication skills - High attention to detail with excellent documentation and organizational abilities - Adaptability to changing priorities and a commitment to quality and service excellence (Note: No additional details of the company were present in the provided job description) Role Overview: At Clario, a part of Thermo Fisher Scientific, you will be a Software Engineer responsible for designing, developing, testing, and maintaining software applications used in regulated clinical trial environments. You will work closely with cross-functional stakeholders to deliver high-quality, compliant solutions. Key Responsibilities: - Analyze, design, develop, test, debug, and maintain software enhancements and new applications using C#, .NET, and SQL - Perform requirements analysis and proactively identify gaps, ambiguities, and risks - Clearly distinguish business requirements from technical design and implementation - Follow established development patterns, coding standards, and software lifecycle processes - Write clear, maintainable code with appropriate unit test coverage - Identify, document, and communicate software defects, including steps to reproduce and workarounds - Conduct code and design reviews to identify weaknesses, alternatives, and trade-offs - Deliver high-quality, tested code on schedule with a low defect rate - Demonstrate application features and fixes to product management and end users - Partner with Quality Assurance by advising on regression testing focus areas - Troubleshoot production and support issues, isolating defects to specific components - Estimate development effort based on detailed design and contribute to planning activities - Adhere to organizational Standard Operating Procedures (SOPs) and regulatory requirements Qualifications Required: - Bachelors degree strongly preferred - 3+ years of professional software development experience - Strong hands-on experience with C#, .NET, and basic SQL - Experience in clinical trials, life sciences, or pharmaceutical environments preferred - Working knowledge of drug development processes and regulatory requirements, including GxP and 21 CFR Part 11 - Proven analytical and problem-solving skills - Ability to work effectively both independently and in a team environment - Strong written and verbal communication skills - High attention to detail with excellent documentation and organizational abilities - Adaptability to changing priorities and a commitment to quality and service excellence (Note: No additional details of the company were present in the provided job description)