ATL01-092425 Validation Specialist – Laboratory CQV & Method Validation - GA jobs in United States
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Validation & Engineering Group, Inc. · 3 months ago

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

Validation & Engineering Group, Inc. (V&EG) is a leading services supplier providing solutions for various industries including Pharmaceutical and Biotechnology. They are seeking a skilled Validation Engineer to support laboratory equipment qualifications and analytical method validations at a manufacturing facility in Johns Creek, GA.

BiotechnologyConsultingProfessional ServicesQuality Assurance

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

Qualification

Laboratory equipment qualificationAnalytical method validationKneat validation lifecycleRisk-based commissioningTechnical writingMicrosoft WordMicrosoft ExcelMicrosoft ProjectCommunication skillsProblem-solving skills

Required

Bachelor's degree in Engineering, Chemistry, or related field
5–7 years of hands-on validation experience in pharmaceutical or medical device industries
Proven expertise in laboratory equipment qualification and method validation
Experience working with Kneat validation lifecycle management system (authoring, reviewing, approving, and archiving documents)
Familiarity with risk-based approaches to commissioning and qualification
Strong technical writing, communication, and problem-solving skills
Proficiency with Microsoft Word, Excel, and Project
Ability to work independently and meet strict timelines

Preferred

Experience in computerized system validation (PLC, HMI)
Knowledge of medical device manufacturing (Class II preferred)
Prior experience with contact lens production platforms

Company

Validation & Engineering Group, Inc.

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Validation & Engineering Group, Proudly serving our clients since 1997.

Funding

Current Stage
Growth Stage
Total Funding
unknown
2025-08-06Acquired

Leadership Team

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Luis Puig
Partner
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Company data provided by crunchbase