Sterile Process Validation Engineer | PPQ & Tech Transfer

Stark Pharma Solutions Inc. in North Carolina is seeking an experienced Process Validation Engineer to support sterile GMP manufacturing projects. You will lead PPQ activities for pre-filled syringe lines, coordinate technology transfer, and ensure cGMP and FDA regulatory compliance across projects. Collaborative work with Manufacturing, Quality, Validation, and Engineering is essential to success. Strong writing and cross‑functional teamwork are essential to deliver robust, compliant processes #J-18808-Ljbffr Stark Pharma Solutions Inc