Quality Assurance Specialist
3 weeks ago
The biopharmaceutical market is experiencing rapid growth, driving the need for high-quality drug production facilities worldwide. As a trusted engineering partner, ZETA Biosystem designs, builds, and automates equipment for aseptic liquid production processes in the biotech and pharmaceutical industries.
Roles & Responsibilities:
Develop and implement Quality Assurance Plans (QAPs) to ensure compliance with industry standards.
Conduct incoming inspections of materials, including plates, pipes, forged materials, flanges, and casting, and record inspection reports.
Review and maintain material MILL TC records in accordance with ASME Code requirements.
Maintain calibration records for QC tools and arrange for instrument calibration from third-party and in-house sources.
Prepare Quality Control Procedures for hydrostatic tests, heat treatment, pneumatic tests, and non-destructive testing.
Inspect fabricated items, including pressure vessels, storage tanks, heat exchangers, and filter housings.
Prepare material identification reports, fit-up reports, material heat charts, NDE reports, pneumatic test reports, and hydro test reports.
PROCESS PIPING:
Conduct P&ID checks and piping stage inspections as per P&ID and process flow.
Verify dead legs as per ASME BPE requirements.
Prepare welding documents, including weld logs, weld samples, and weld print sheets.
Conduct live and final borescope inspections of weld joints for defects and discoloration, and prepare reports.
Prepare piping documents, including piping material charts, valve material charts, and bought-out component certificates.
WELDING:
Develop WPS, PQR, and WPQ documents for GTAW, FCAW, and orbital welding as per ASME IX and EN 15614 requirements.
Select welding consumables in accordance with ASME Code requirements.
NDE:
Certified Level II NDT Engineer (UT, PT, RT, VT)
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