Quality Assurance Quality Control Inspector

Job Title: QA/QC Technician - NDT VT (Level II Inspector) Job Location: Must be Job Type(s): Full-time | Contract (contract-to-hire, possibility) Job Opportunity(s): Immediate Need | Multiple Openings Job Summary: The QA/QC Technician and/or ASNT NDT Visual Testing (VT) Level II Inspector supports pharmaceutical and biotechnology manufacturing operations by performing visual inspections in accordance with applicable industry codes (ASME, AWS), GMP requirements, and project quality standards. The role focuses on high-purity process piping, clean utilities, pressure systems, and related structural components to help ensure compliance with regulatory, safety, and quality requirements. Inspection & Testing Responsibility Overview: Perform VT Level II inspections on high-purity stainless steel piping (e.g., 316L), clean utilities (WFI, PW, Clean Steam), pressure vessels, tanks, skids, and supports. Verify weld profiles, surface finish, alignment, fit-up, and overall workmanship. Confirm work meets applicable project specifications and quality requirements. Documentation, GMP & Validation Support Responsibility Overview: -Complete GMP-compliant inspection documentation, including inspection test records (ITRs), weld logs, and nonconformance reports (NCRs). -Ensure records are accurate, complete, and suitable for audits. -Support system walkdowns, punch-list resolution, and quality audits as needed. Quality & Regulatory Compliance Responsibility Overview: -Identify defects that could affect product quality, cleanability, sterility, or system integrity. -Follow site quality systems and GMP practices. Preferred Minimum Qualifications: -ASNT NDT VT Level II certification (current or previously held). -3 to 5+ years of relevant experience in pharmaceutical or biotech environments. -Hands-on experience inspecting high-purity stainless steel welds. -Additional NDT certifications (PT, MT, and/or UT) are a plus. -Familiarity with FDA 21 CFR Parts 210/211, EU GMP Annex 1, and ISPE Baseline Guides. Work Environment: On-site role at pharmaceutical or biotech manufacturing facilities. May involve extended hours, weekend work, or travel. EOE