QC Engineer (Analytical Systems CSV)

Role Overview

We are seeking a QC Engineer with strong experience in Computer System Validation (CSV) for analytical laboratory instruments / equipment. The role ensures compliance with 21 CFR Part 11, data integrity, and global validation standards in a regulated GMP environment.

Key Responsibilities

• Lead CSV activities for analytical equipment or instruments and lab computerized systems (e.g., HPLC, GC, UV, LIMS, Empower).
• Develop and execute validation deliverables : URS, risk assessments, IQ / OQ / PQ, RTM, and summary reports.
• Ensure compliance with 21 CFR Part 11, Annex 11, ALCOA+ principles, and data integrity controls.
• Evaluate and validate audit trails, security settings, and user access controls.
• Support integration between instrument, PC, network, and enterprise systems.
• Draft, review, and maintain SOPs, validation documentation, and audit readiness materials.
• Contribute to lifecycle management of systems including periodic reviews, upgrades, and change control.
• Collaborate with QA, QC, and IT to support inspection readiness and continuous improvement.

Requirements

Requirements