IT Manufacturing Quality/Validation Analyst - Onsite/Hybrid in Greenville, NC

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