Job Description
Confluent Medical Technologies is dedicated to working collaboratively with our customers, taking their projects from rapid prototype into high volume production.
Our unparalleled technical expertise, proven experience and partnership with our clients has allowed us to perfect the process necessary to deliver world-class medical devices through innovative material science, engineering, and manufacturing.
Our primary capabilities include : Nitinol components, balloon expandable stents and balloon catheters, delivery systems, biomedical textiles, access kits, and guidewires.
We take pride in our position as the leader in the medical technology space and are driven by a passion to create products that our clients have envisioned for their customers.
We are looking for a Manufacturing Engineer II to join our team. As a uniquely qualified candidate, you will be responsible for production planning and inventory control for multiple products while prioritizing operations to ensure maximum performance and minimum delay.
This individual will take a lead role in continuous improvement, product flow and capacity improvement to improve the overall efficiency of manufacturing while service level targets.
As a uniquely qualified candidate, you will :
Responsible for all aspects of process development - specifically related to wire, strip and tube processing. Develop and or improve processes to meet customer functional requirements.
Plan and conduct work requiring judgment in the independent evaluation, selection, and adaptation and modification of the processing of nitinol materials-focusing on the processing of wire, strip and tube.
Document process development activities in technical memorandums and other process related documents. Interface with internal program managers and external customers to understand a comprehensive knowledge of new products.
Work in collaboration with operators, technicians, and process engineers to deliver materials products that meet customer requirements.
Coordinate with production team for training and manufacturing of nitinol materials. Partner with other Development Engineers to develop strategic processing goals and objectives in order to integrate processes into to LEAN value streams.
May technically supervise or coordinate the work engineers, draftspersons, technicians, and others who assist in specific assignments.
Develop an expertise in nitinol materials!
Qualifications / Requirements : Bachelor’s degree in Engineering with a minimum of 2-5 years of related engineering experience.
BA or BS in non-engineering field with 5 to 10 years of medical related engineering experience. Ability to communicate clearly and efficiently in a highly technical environment.
Possess excellent communication skills - both written and oral. Knowledge of Excel, statistical process control software Highly motivated and independent.
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