Senior Validation Engineer: Pharma Quality & Compliance

Kindeva Drug Delivery in Lexington, Kentucky, is looking for a Validation Engineer. This role ensures compliance with FDA and global regulations in pharmaceutical manufacturing processes. Responsibilities include developing validation protocols, supporting commissioning activities, and maintaining documentation. Candidates should have a Bachelor’s degree in engineering or life sciences and at least 5 years of relevant experience. Familiarity with automated systems and validation tools is preferred.

Kindeva is committed to quality and continuous improvement in a fast-paced environment.
#J-18808-Ljbffr