QAQC Technician-NDT VT Level II Inspector
Listed on 2026-05-16
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Quality Assurance - QA/QC
Quality Technician/ Inspector, Quality Control / Manager, Quality Engineering, QA Specialist / Manager
NDT VT LEVEL II INSPECTOR: FST Technical Services
FST Technical Services was founded in 1984 to serve the needs of the semiconductor, microelectronics, and life sciences industries. We are growing a new QAQC team for a project based in Vacaville, CA at a pharmaceutical facility build, and we are seeking immediate support from experienced NDT VT Level II Inspectors.
QAQC Technician / NDT VT Level II InspectorJob 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.
- Complete GMP‑compliant inspection documentation including ITRs, weld logs, and NCRs.
- Ensure documentation is accurate, complete, and audit‑ready.
- Participate in system walk‑downs, punch list resolution, and audits.
- Identify defects impacting product quality, cleanability, sterility, or system integrity.
- Adhere strictly to GMP and site quality systems.
- 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.
On‑site role at pharmaceutical or biotech 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.
Hourly pay rate range: $35/HR to $50/HR – based on experience.
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