Validation Engineer

Validation & Engineering Group; Raleigh (NC); On-site; USD 80,000 - 100,000; Full time

Job summary

A leading services supplier in the pharmaceutical and biotechnology sector is seeking a highly motivated Validation Engineer to support validation activities. The role involves ensuring equipment and processes comply with regulations to maintain product quality. Candidates should have a Bachelor's degree in Engineering or a related field, with 5+ years of validation experience. Key responsibilities include executing validation protocols and collaborating with cross-functional teams. The position is located in Raleigh, North Carolina.

Qualifications

• 5+ years of experience in validation within regulated industries.
• Hands-on experience with manufacturing equipment and laboratory instruments.
• Strong knowledge of GMP, GLP, and regulatory guidelines.

Responsibilities

• Plan, develop, and execute validation protocols for equipment and systems.
• Support validation of laboratory instruments and production equipment.
• Draft and review validation documents, ensuring compliance.

Skills

Validation protocols (IQ, OQ, PQ)

GMP

Regulatory compliance

Analytical skills

Technical writing

Cross-functional collaboration

Education

Bachelor’s degree in Engineering, Life Sciences, or related field

Job description

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.

Job Description

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.
• 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.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or related field.
• 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.
• 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.
• Knowledge of risk-based validation approaches (e.g., ASTM E2500).

Additional Information

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