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ATL01-121724 Validation Engineer – Cold Room Qualification (NC)

Validation & Engineering Group, Inc
Greenville, NC Full Time
POSTED ON 1/17/2025
AVAILABLE BEFORE 3/18/2025

Department : Field - USA Location : Greenville, NC

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Validation & Engineering Group, Inc. (V&EG) is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas : Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position :

  • Validation Engineer

Job Description :

We are seeking a skilled Validation Engineer to perform the full qualification of a cold room (2-8°C) for a regulated FDA production site. The engineer will be responsible for executing qualification protocols, ensuring compliance with GMP standards, and delivering comprehensive documentation.

Key Responsibilities :

  • Develop and execute protocols : IQ, OQ, PQ, and validation studies (Empty Chamber, Full Chamber, Open Door).
  • Author and finalize Validation Plans, Summary Reports, and associated documentation.
  • Perform Installation Verification (IV) and Operational Verification (OV).
  • Conduct training on client systems and SOPs.
  • Use Kneat software for documentation and protocol management.
  • Collaborate with client teams to meet project timelines and deliverables.
  • Qualifications :

  • Bachelor’s degree in Engineering, Life Sciences, or related field.
  • 3 years of validation experience in GMP-regulated environments.
  • Strong experience in cold room qualifications and thermal mapping studies.
  • Proficiency with Kneat software (required).
  • Strong understanding of FDA regulatory requirements and GMP standards.
  • Ability to work independently and meet project deadlines.
  • START YOUR APPLICATION

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