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:

• Computer System Validation (CSV) Specialist

Job Summary
We are seeking a Computer System Validation (CSV) Specialist with more than five years of experience in the biotech industry to support validation activities for regulated computerized systems. The ideal candidate has hands-on experience using Kneat and is well-versed in CSV requirements within GMP environments.

Key Responsibilities

• Support planning, execution, and documentation of computer system validation activities

• Develop, execute, and review CSV lifecycle documentation

• Ensure computerized systems comply with GMP and regulatory requirements

• Support risk assessments, testing, and validation reports

• Collaborate with IT, Quality, and Engineering teams

Required Qualifications

• Bachelor’s degree in Engineering, Computer Science, or related field

• More than 5 years of experience in Computer System Validation within biotech or pharmaceutical environments

• Hands-on experience using Kneat

• Strong knowledge of GMP, CSV, and data integrity requirements