IT Manufacturing Quality/Validation Analyst - Onsite/Hybrid in Greenville, NC
Job in
Wilmington, New Hanover County, North Carolina, 28412, USA
Listed on 2026-09-22
Listing for:
Socket.dev
Full Time
position Listed on 2026-09-22
Job specializations:
-
Quality Assurance - QA/QC
IT QA Tester / Automation, QA Specialist - Analyst/Manager, Data Analyst
Job Description & How to Apply Below
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 SummaryWe 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.
- 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.
- Onsite/Hybrid in Greenville, NC
- Pay rate : $48 on C2C or $42 W2
- Interviews:
Video interviews. - Docs required: will be required.
- Availability:
Candidates able to join immediately are preferred
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