CSV Validation Engineer - GMP & CQV Specialist
Listed on 2026-09-30
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Engineering
Quality Engineering, Pharma Engineer, Regulatory Compliance Specialist -
Quality Assurance - QA/QC
Quality Engineering, Regulatory Compliance Specialist
Intellectt Inc is seeking a Computerized System Validation Engineer I in Social Circle, Georgia, to support validation activities for computerized systems used in pharmaceutical manufacturing. The role is focused on ensuring compliance with GMP, quality, safety, and regulatory standards.
Key responsibilities include preparing validation documents, assisting in system testing, supporting change controls, and participating in risk assessments. Candidates should have a Bachelor’s degree in Engineering and familiarity with pharma regulations and validation protocols.
Consider building your career as a CSV Validation Engineer - GMP & CQV Specialist at Intellectt Inc.
Are you ready to take on the CSV Validation Engineer - GMP & CQV Specialist role at Intellectt Inc?
We would love to welcome a new CSV Validation Engineer - GMP & CQV Specialist to our organisation in GA, United States.
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