This position provides technical leadership in the development, optimization and sustaining of manufacturing processes for medical devices in accordance with Getinge’s Quality system and regulatory requirements (ISO 13485 and FDA 21 CRF Part 820). This individual is a key resource during Design for Manufacturability (DFM), collaborating closely with cross-functional teams to ensure current and new products are scalable, robust, cost-effective, and production-ready. Leadership cross-functional initiatives, drive strategic improvements, oversee process validations, implement continuous improvement strategies, and support commercial-scale operations.
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Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees