NDT VT LEVEL II INSPECTOR: We are growing a new QAQC team for a project based in Vacaville, CA at an exciting pharmaceutical facility build! We are seeking immediate support from experienced NDT VT Level II Inspectors with a history of working a pharmaceutical, semiconductor, data center, or other high-tech facilities.
This opportunity that with excellent pay, strong benefits and a healthy travel/per diem package for travelling resources. Project location is Vacaville, CA.QAQC Technician/NDT VT Level II Inspector
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-ready.
- Participate 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 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.
If you are looking for a professional, challenging and stimulating environment and meet the above criteria, APPLY NOW!!!
Hourly pay rate range: $35/HR to $50/HR - based on experience
