ATL01-092425 Validation Specialist - Laboratory CQV & Method Validation - GA

Position Overview

We are seeking a skilled Validation Engineer to support a critical project at a manufacturing facility in Johns Creek, GA. The consultant will focus on laboratory equipment qualifications and analytical method validations to enable implementation of new products in production. This is a client-facing, hands-on role requiring strong technical expertise, attention to detail, and ability to work independently.

Location : Johns Creek, GA

Duration : October 20, 2025 – January 9, 2026

Commitment : Full-time (40–45 hours / week)

Key Responsibilities

• Plan, author, and execute qualification protocols (IQ / OQ / PQ) for new laboratory instruments, including TruScans and balances
• Develop and execute validation protocols for ~11 analytical methods (e.g., Gas Chromatography, UV-Vis Spectroscopy, Karl Fischer Titrations
• Generate and revise validation documentation (protocols, reports, SOPs, specifications) in compliance with cGMP standards.
• Conduct investigations for deviations, perform root cause analysis, and implement corrective actions.
• Ensure compliance with Good Documentation Practices (GDP) and "right the first time" deliverables.
• Collaborate with cross-functional teams (QA, Engineering, Production) and communicate project status to stakeholders.
• Support change control management and risk assessment activities.

Required Qualifications

Qualifications

Additional Information

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