Performs engineering work related to planning, devising, or adapting methods to improve process effectiveness at captive and third party manufacturing sites.
Examines components, equipment, processes, operations, and finished device design to identify improvement opportunities.
Drive product and process improvements in support of Insulet’s CAPA system.
Generate validation/qualification protocols, coordinate the execution of the validation/qualification protocols and write validation/qualification final reports.
Author and implement Engineering Change Orders.
Design and coordinate the construction manufacturing fixtures.
Support responsibility for all project phases from concept, specification, cost justification, project management, installation, training, qualification, implementation into manufacturing, and support.
Perform other duties as assigned.

Bachelors of Science in Engineering discipline and/or equivalent combination of education and experience.
3-5 years’ work experience in a manufacturing environment is required.
Experience in the medical device industry is preferred.
Effective verbal and written communication skills.
Ability to organize and judge priorities.
Ability to generate and maintain accurate records.
Ability to work well in a team environment with the ability to take personal ownership of projects as needed.
Manufacturing process knowledge (Injection Molding, Metal Stamping/forming, PCB manufacture, Manual and automated assembly, decorating, extrusion and ultrasonic welding) a plus.
Strong computer skills; MS Office / MS Project / Statgraphics.
CAD (ProEngineer / Solidworks) experience desirable.

Manufacturing Engineer

Key skills