Job Description

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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

• Bachelor's degree in Chemistry, Life Sciences, Engineering, or related discipline.
• 5-10 years' experience in analytical instrument/equipment CSV within pharmaceutical/biotech QC labs.
• Strong knowledge of cGMP, GAMP 5, 21 CFR Part 11, Annex 11.
• Hands-on experience with microbiology analytical equipment is an advantage.
• Familiarity with electronic validation tools (e.g., Kneat) is preferred.
• Strong documentation, troubleshooting, and cross-functional collaboration skills.

Skills Required