A company is looking for a Validation Engineer to support validation activities across various systems and processes.
Key Responsibilities
Generate and execute validation lifecycle documentation for GMP regulated assets
Support validation activities for tech transfer projects, including authoring and executing validation documents
Write and revise qualification and verification documents, and prepare summary reports for validation activities
Qualifications and Requirements
Bachelor's degree in a life science, engineering, or related technical field
4-7 years of experience in the biotech, pharmaceutical, or medical device industry
Strong knowledge of FDA cGMP requirements and risk-based validation principles
Hands-on validation experience in equipment and computerized systems
Experience generating protocols for automated production systems
Validation Engineer • Dallas, Texas, United States