Sterile Validation Engineer — GMP​/FDA Compliance Champion

A pharmaceutical company in Sacramento is seeking a Validation Engineer responsible for ensuring compliance with regulatory requirements and industry standards in sterile manufacturing processes. You will lead the validation lifecycle from installation through qualification, conduct process validation studies, and prepare necessary documentation. Candidates should possess a Bachelor's degree and a minimum of 2 years of experience in a related role.

The position offers a salary range of $90,000 to $105,000 plus benefits.
For the Sterile Validation Engineer — GMP/FDA Compliance Champion position at Nivagen Pharmaceuticals, Inc., we are reviewing applications now. Are you ready to take on the Sterile Validation Engineer — GMP/FDA Compliance Champion role at Nivagen Pharmaceuticals, Inc.? We would love to welcome a new Sterile Validation Engineer — GMP/FDA Compliance Champion to our team in Sacramento, CA, United States.