About this role
IT Manufacturing Quality/Validation Analyst - Onsite/Hybrid in Greenville, NC
We are looking to hire a candidate with the mentioned skill sets and experience for one of our clients within the pharmaceutical Industry. This is a 12 month contracting role, with potential for extension
Job Summary
We are seeking an IT Manufacturing Validation Analyst to support validation, quality, automation, and compliance activities within a manufacturing environment. The ideal candidate will have hands-on experience with IT/Manufacturing validation, Quality processes, CAPA, test automation, and data visualization.
Key Responsibilities
• Support IT and manufacturing validation activities for systems, applications, and automated processes.
• Develop and execute validation documentation, test plans, test scripts, test cases, and validation protocols.
• Support Quality Assurance (QA) activities, including testing, defect tracking, investigation, and resolution.
• Participate in CAPA (Corrective and Preventive Action) activities and help ensure timely remediation and documentation.
• Perform validation and testing of manufacturing-related applications and systems.
• Support test automation using tools such as UiPath and Microsoft Power Automate.
• Develop, execute, and maintain automated testing workflows for manufacturing/IT applications.
• Collaborate with IT, Manufacturing, Quality, Engineering, and business teams to ensure systems meet quality and compliance requirements.
• Analyze testing and operational data and create Power BI dashboards and visualizations to support quality and manufacturing reporting.
• Maintain appropriate validation and quality documentation in accordance with established procedures and compliance requirements.
• Identify process improvements and opportunities to increase testing and validation efficiency through automation.
Required Qualifications
• 5+ years of IT, validation, quality, QA, or related experience.
• Hands-on experience with IT/Manufacturing validation
• Experience in Quality Assurance, testing and validation within a manufacturing or regulated environment.
• Experience with CAPA processes.
• Hands-on experience with automation tools, preferably UiPath and Power Automate.
• Experience with software/application testing and test documentation.
• Hands-on Power BI experience, including dashboards, reporting, and data visualization.
• Strong analytical, documentation, communication, and problem-solving skills.
• Ability to work effectively with cross-functional IT, manufacturing, quality, and business teams.
• Experience in pharmaceutical, biotechnology, medical device or other regulated manufacturing environments.
• Knowledge of GxP, CSV, GMP or related regulatory/compliance requirements.
• Experience with automated testing frameworks and QA automation.
• Familiarity with electronic quality management systems and change-control processes.
Other details
• Onsite/Hybrid in Greenville, NC
• Pay rate : $48 on C2C or $42 W2
• Interviews: Video interviews.
• Docs required: ID proof will be required.
• Availability: Candidates able to join immediately are preferred