VTI Life Sciences seeks a forward‑thinking Medical Device Quality Engineer for a contract role to lead validation execution with operations and engineering on special processes such as laser marking and laser welding.
The successful candidate will review IQ/OQ/PQ protocols, generate validation packages, support SOP development, and contribute to deviation investigations; 2+ years GMP experience in medical devices is required.
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For the Medical Device Quality Engineer: Validation Specialist (Contract) position at Inc. (Vti), we are reviewing applications now.
The following opening is for a Medical Device Quality Engineer: Validation Specialist (Contract) with Inc. (Vti).
Our organisation is growing, and we are hiring a Medical Device Quality Engineer: Validation Specialist (Contract) in Pendleton, England, United Kingdom.
This opening is for the Medical Device Quality Engineer: Validation Specialist (Contract) role at Inc. (Vti).