Job Description

ALTEN Technology USA is seeking a Validation Engineer II to ensure the highest standards of sterilization validation in a pharmaceutical cleanroom environment. The role involves developing and executing validation protocols, performing aseptic lab practices, and collaborating with cross-functional teams.

Responsibilities

• Develop and execute sterilization validation protocols
• Perform aseptic lab practices and cleanroom operations
• Handle biological indicators and monitor VHP cycles
• Interpret microbial results and prepare validation reports
• Collaborate with cross-functional teams

Requirements

• Bachelor’s degree in Engineering, Microbiology, or related field
• 2–4 years of experience in pharmaceutical validation or sterilization processes
• Familiarity with sterilization principles, aseptic techniques, and cleanroom practices
• Knowledge of biological indicators, VHP cycles, and microbial result interpretation
• Strong understanding of cGMP and FDA guidelines

Benefits

• No benefits