Job Summary: Support engineering functions in the development and manufacturing of surgical instrumentation while maintaining compliance in a regulated environment.
Learn MoreJob Summary: The Quality Control inspector will provide mechanical inspection of all products, components and records and adhere to quality system policies.
Learn MoreJob Summary: Effectively supervise ECA Medical’s second shift production operations to achieve quality, schedule, and performance goals.
Learn MoreJob Summary: The Injection Molding Process Engineer is responsible for developing injection- molding processes and products to support new product launches and optimizing existing molding processes. This person will be working closely with Product Development Engineering, Mold Development Team, Production, Manufacturing Engineering, Supply Chain, Quality, and the Sales team: to facilitate the release of new products into production and changes to existing products as process improvements. This person is expected to foster a positive and professional work environment that is fully committed to continuous improvement and lean principles.
Learn MoreJob Summary: This position serves as an inside sales and support administrator for ECA Medical Instruments. Candidate manages all backend customer requirements and support functions including inside sales, order processing and entry, inventory management, customer support, sales process and operations, and selected marketing support activities.
Learn MoreJob Summary: The Sr. Product Development Engineer (PDE) is actively engaged in executing the main elements of New Product Realization to introduce to market novel surgery-ready surgical instruments. As a team member in this role, you will participate with the following activities: Concept Development, Design & Development, Performance Evaluation, Design Verification & Validation, and Design Transfer. You will serve as Core Team Member from Product Development, partnering with cross-functional SME on projects. This role includes both hands-on activities and planning, with a focus on innovation, execution, and efficiency. To support development of successful products, you will partner with Marketing / Sales to understand the User Needs and define Design Input. These can be obtained during Voice of Customer meetings and cadaveric / Sawbones labs. During the initial concept development, you will review the Intellectual Property landscape and determine new IP that should be filed. During this phase, prototypes are made and evaluated to assess feasibility and functionality of various design and material. As the project evolves and the product design is refined, you will create engineering drawings with close input from Manufacturing and Quality to obtain feedback on DFM and Inspection methodology. You will lead the team to ensure relevant CTQ’s are selected based on features critical to product functionality. You will work closely with Manufacturing Engineering to assist in the development of the assembly line. If required, you will oversee the development of packaging solutions once the product design is finalized. As the product design is frozen, you will particiate in the planning and execution of Design Verification & Validation activities. You will be responsible to author the Design V&V documentation and participate in activities including product & packaging performance evaluation, Biocompatibility assessment, and Sterilization Validation assessment. Throughout the V&V Phase, you will participate in a well-planned and organized Design Transfer of the product design & specifications to production. You will partner and work closely with Operations, Supply Chain, Quality, and Manufacturing throughout this process to ensure the Design Transfer is completed thoroughly and in time to start production.
Learn MorePOSITION REPORTS TO: Assembly Supervisor/Manager POSITION OBJECTIVE: Effectively assemble cleanroom devices per specific work instructions and or all required documentation within work order package. This is a temporary assignment.
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