GSK seeks a seasoned quality/regulatory leader for medical devices within combination products. The role focuses on risk management, design and development file oversight, and post-market quality activities. You will collaborate across functions to uphold regulatory standards and drive continuous improvement.
Ideal candidates have extensive QMS/cGMP experience, strong investigations skills, and will lead inspections and supplier quality efforts in a hybrid onsite setting.
#J-18808-LjbffrSenior Device Quality Engineer — Hybrid Onsite Medical Devices in zebulon at Unknown Company
This position is listed as full time and hybrid.