For one of our clients, an international medtech company, we are looking for a Process Validation Engineer to join the Quality & Regulatory organization.
This role focuses on qualification and validation activities for manufacturing processes.
Context
You will join the Quality & Regulatory organization and contribute to the qualification and validation strategy for internal and external manufacturing processes. Working closely with R&D, Operations, Regulatory Affairs, Production, Engineering, suppliers and subcontractors, you will ensure that manufacturing processes are robust, compliant and inspection-ready.
Responsibilities
As Process Validation Engineer, you will:
Required Profile
You have an engineering degree, ideally in Mechanical Engineering, with proven experience in validation and qualification processes within a regulated environment.
You bring at least 5 years of experience in additive manufacturing using metallic materials, ideally in medical devices, orthopaedics, spinal implants or implantable devices.
You also bring:
Preferred
Experience with subcontractors, external manufacturing partners, cleanroom systems or environmental monitoring is a plus. A Lean certification or demonstrated experience in Lean Manufacturing / continuous improvement is also preferred.
Work Location: Hybrid remote in Geneva, GE
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