QAQC Technician-NDT VT Level II Inspector

FST Technical Services•Vacaville, CA

4d•Onsite

About The Position

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 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, NC. 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.

Requirements

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.
Familiarity with FDA 21 CFR Part 210/211, EU GMP Annex 1, ISPE Baseline Guides.
Authorized to permanently work in the USA.

Nice To Haves

Additional NDT certifications (PT, MT, UT).

Responsibilities

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 walkdowns, punch list resolution, and audits.
Identify defects impacting product quality, cleanability, sterility, or system integrity.
Adhere strictly to GMP and site quality systems.