The Staff External Manufacturing Engineer is responsible for functioning as an integral member of a team in support of manufacturing operations performed by external manufacturers, providing technical services to insure quality, cost and performance objectives are met.
In this role, you will manage all phases of medical device design and development projects from concept through clinical trials in accordance with Healthcare design control procedures, ensuring projects are completed on time and within budget.
In this role, the selected candidate will oversee project Delivery process with key contributors to help manage scope and prepare change requests - including tasks, deliverables, milestones, resources, and estimated costs; act as primary point of contact for the client(s) throughout the project life-cycle.
In this role, you will manage all phases of medical device programs from initiation through production handover, ensuring programs are completed on time, within budget and meeting all client/Nypro and regulatory requirements.
In this role, you will participate in evaluation and selection of applications and implementation with partners/vendors and identify potential risks/issues and create strategies for contingency planning and risk mitigation.
In this role, you will lead continuous improvement efforts and adopt industry best practices to enhance the tools and systems for managing field inventory; Serve as the regional leader for implementation.
In this role, you will manage the technical challenges of technology application and new product or business introduction; identifies, communicates, and manages moderate to high levels of technical risk.