QAQC Technician-NDT VT Level II Inspector

QAQC Technician / NDT VT Level II Inspector FST Technical Services was founded in 1984 to serve the needs of the growing, worldwide Semiconductor/Microelectronics and Life Sciences industries. We began as an independent interface between our clients and their subcontractors to establish build‑clean installation methods that satisfied internal specifications and conformed to regulatory requirements. We are looking for Experienced QAQC Technicians to join our team in Holly Springs, NC. This position is local, so we are seeking candidates within a commutable distance to the greater Holly Springs, NC area. Job Summary The QAQC Technician and/or ASNT NDT VT Level II Inspector supports pharmaceutical and biotechnology manufacturing facilities by performing Visual Testing (VT) inspections in accordance with ASME, AWS, GMP, and client‑specific quality standards. The role focuses on high‑purity process piping, clean utilities, pressure systems, and structural components to ensure compliance with regulatory, safety, and quality requirements. Inspection & Testing (Pharma‑Specific) Perform VT Level II inspections on high‑purity stainless steel piping (316L), clean utilities (WFI, PW, Clean Steam), pressure vessels, tanks, skids, and supports Verify weld profiles, surface finish, alignment, fit‑up, and workmanship Ensure compliance with project specifications Documentation, GMP & Validation Support Complete GMP‑compliant inspection documentation including ITRs, weld logs, and NCRs Ensure documentation is accurate, complete, and audit‑readyParticipate in system walkdowns, punch list resolution, and audits Quality & Regulatory Compliance Identify defects impacting product quality, cleanability, sterility, or system integrity Adhere strictly to GMP and site quality systems Preferred Qualifications ASNT NDT VT Level II certification from current or previous employer 3–5+ years experience in pharmaceutical or biotech facilities Experience inspecting high‑purity stainless steel welds Additional NDT certifications (PT, MT, UT) Familiarity with FDA 21 CFR Part 210/211, EU GMP Annex 1, ISPE Baseline Guides Work Environment On‑site role at pharmaceutical or biotechnology facilities. May include extended hours, weekends, or travel. All parties authorized to permanently work in the USA are encouraged to apply. We are unable to sponsor at this time. No third‑party candidates considered for this position. APPLY NOW!!! #J-18808-Ljbffr