[Hiring] Associate Software Quality & Test Analyst @Parexel

Role Description

We are seeking an Associate Software Quality and Test Analyst (Software Quality Analyst, Test Analyst, Computer System Validation Analyst) to join our life sciences and clinical research team. As an Associate Software Quality and Test Analyst, you will support software quality, system validation, testing, and compliance activities for regulated business applications. This position plays a key role in validation deliverables, change requests, test case creation and execution, and quality documentation, helping ensure that systems remain compliant and audit ready.

You'll collaborate with business, IT, Quality, and vendor teams, follow industry-standard processes, and contribute to system enhancements and projects. Responsibilities include:

• System validation support
• Test execution
• Quality documentation
• Change request support
• Traceability

You'll join a fast-paced, growth-oriented environment focused on making a meaningful impact through validation, testing, and quality activities that keep systems compliant, traceable, and inspection ready. Your work helps protect data integrity and the reliability of the systems that support the delivery of new therapies to patients. With diverse teams and continuous learning opportunities, the Associate Software Quality and Test Analyst can explore career paths and expand skills across clinical research.

Qualifications

• Bachelor's degree in information technology, Computer Science, Life Sciences, Engineering, or a related field
• 1-3 years of experience in software testing, validation, quality assurance, or related roles
• Understanding of the Software Development Life Cycle (SDLC), software testing methodologies, and user acceptance testing (UAT) processes
• Strong analytical, documentation, and problem-solving skills
• Excellent verbal and written communication skills

Requirements

• Strengths in software testing and UAT, system validation, and quality documentation
• An understanding of regulated environments and the documentation and compliance standards they require
• The ability to collaborate across teams and communicate clearly
• A patient-focused mindset and strong attention to detail
• Comfort working with change management and defect tracking processes

Preferred Qualifications

• Experience with Computer System Validation (CSV)
• Knowledge of Good Practice (GxP), Good Automated Manufacturing Practice (GAMP 5), and FDA 21 CFR Part 11 (Electronic Records and Electronic Signatures) requirements
• Experience with change control and quality management processes
• Familiarity with tools such as Jira, ServiceNow, HP ALM, and similar tools

Benefits

• Flexibility
• Growth opportunities
• A supportive team environment