Validation Engineer

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 highly motivated Validation Engineer to support validation activities within regulated industries such as Pharmaceuticals, Biotechnology, Medical Devices, Chemicals, or Food Manufacturing
. The Validation Engineer will ensure equipment, systems, and processes meet regulatory requirements and function reliably to maintain product quality and patient safety.

Key Responsibilities

• Plan, develop, and execute validation protocols (IQ, OQ, PQ) for equipment, utilities, facilities, and manufacturing systems.
• Support validation of laboratory instruments, production equipment, cleaning processes, and computerized systems.
• Ensure compliance with cGMP, FDA, EMA, and other applicable regulatory guidelines
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• Draft and review validation documentation, including protocols, reports, SOPs, and risk assessments.
• Perform troubleshooting and root cause analysis for validation or equipment-related deviations.
• Collaborate with cross-functional teams (Engineering, Quality, Manufacturing, Laboratory) to support project deliverables.
• Participate in change control, CAPA, and continuous improvement initiatives.
• Maintain accurate records and ensure documentation is audit-ready at all times.

• Bachelor’s degree in Engineering, Life Sciences, or related field
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• 5+ years of experience in validation within pharmaceutical, biotechnology, or related regulated industry.
• Hands-on experience with validation of manufacturing equipment, laboratory instruments, and/or computerized systems.
• Strong knowledge of GMP, GLP, and regulatory guidelines
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• Excellent analytical, organizational, and technical writing skills.
• Ability to work independently and in cross-functional teams.

Preferred Skills

• Experience with cleaning validation, sterilization, utilities (HVAC, water, compressed gases).
• Familiarity with data integrity and 21 CFR Part 11 compliance
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• Knowledge of risk-based validation approaches (e.g., ASTM E2500).

All your information will be kept confidential according to EEO guidelines.