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ATL01-092425 Validation Specialist – Laboratory CQV & Method Validation - GA Job Opening In USA, USA – Now Hiring Validation & Engineering Group, Inc


Job description

Department: Field - USA Location: , GA
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Validation & Engineering Group, Inc.

(V&EG)
is a leading services supplier providing solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the areas of Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other technical services.

  • Validation Engineer – Laboratory & Method Validation
  • Location: Johns Creek, GA

    Duration: October 20, 2025 – January 9, 2026

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

    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.

    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

  • 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 Qualifications

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

  • Position requires onsite presence in Johns Creek, GA.
  • Contractor must complete required onboarding and training prior to project start.
  • START YOUR APPLICATION

    Required Skill Profession

    Life, Physical, And Social Science Technicians


    • Job Details

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