Manufacturing Engineer II
4 months ago
We value what makes you unique. Together, we can change healthcare worldwide. At Medtronic, we push the limits of what technology can do to help alleviate pain, restore health, and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be. Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations
A Day in the Life
In this exciting role as anEngineer II in the Bedford facility you will have responsibility for supporting the manufacture of high-quality and complex catheters to support the Cardiac Ablation Solutions Business. In this role you will be part of a team that grows the operations capacity over 5X to support our customer needs in this newly acquired product portfolio. You will support improvements in manufacturing quality, capacity, and stability through solving problems, developing solutions, and executing strategies.
* This role is our 3rd shift Monday-Friday, 10:00pm-6:30am EST.
Responsibilities may include the following and other duties may be assigned.
Designs manufacturing processes, procedures and production layouts for assemblies, equipment installation, processing, machining and material handling. Designs arrangement of machines within plant facilities to ensure most efficient and productive layout. Designs sequence of operations and specifies procedures for the fabrication of tools and equipment and other functions that affect product performance. Adapts machine or equipment design to factory and production conditions. May incorporate inspection and test requirements into the production plan. Inspects performance of machinery, equipment, and tools to verify their efficiency, and investigates and initiates corrective action of problems and deficiencies to ensure product quality. Develops manufacturing processes that are applicable to statistical process control, and may develop those techniques. Provides guidance to engineering regarding design concepts and specification requirements to best utilize equipment and manufacturing techniques. Ensures processes and procedures are in compliance with regulations. Must Have: Minimum RequirementsBachelors degree required Minimum of 2 years of relevant experience, or advanced degree with 0 years of experience Nice to Have Medical Device or regulated industry experience Experience managing Quality System Process Documents Experience understanding proper documentation/quality requirements for a regulated environment Experience Process and equipment Validation and Qualification (IQ,OQ,PQ) Experience with automation, vision, PLC processes Strong problem-solving skills Project management experience Strong written and verbal communication skills
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