Syner-G is seeking a Sr. Validation Engineer to lead validation activities across equipment, utilities, facilities, and computerized systems within GMP environments. You will develop and manage validation lifecycle documentation, provide guidance to junior staff, and ensure regulatory alignment across projects. Qualified candidates have 7–11 years in biotech/pharma, strong FDA cGMP knowledge, and expertise in CSV, IQ/OQ/PQ, and risk-based validation principles.

Also on the board Same function, level within a rung

Level

Lead

Location

Hillsboro, IL

Occupation

Validation Engineers

Industry

Pharmaceutical Preparation Manufacturing

Posted

9 days ago

Apply for this role →