Engineer III, Process
Job Requisition #: 11802
Date Posted: 10/05/2011
Category: Leads Development
Location: Sylmar - CA - USA
About Us
St. Jude Medical develops medical technology and services that focus on putting more control into the hands of those who treat cardiac, neurological and chronic pain patients worldwide. The company is dedicated to advancing the practice of medicine by reducing risk wherever possible and contributing to successful outcomes for every patient. St. Jude Medical is headquartered in St. Paul, Minn. and has four major focus areas that include: cardiac rhythm management, atrial fibrillation, cardiovascular and neuromodulation.
We are an Equal Opportunity/Affirmative Action Employer. Our Cardiac Rhythm Management business unit, located in the suburbs of Los Angeles, is currently seeking the following professional:
Job Overview
Engineer III, Process
Summary Working without appreciable supervision, designs and implements manufacturing processes, instrumentation and equipment and assists in resolving related problems. Work requires the application of theoretical principles and creative/analytical techniques typically acquired in a recognized four-year or more academic course of study. Applies advanced engineering and scientific principles to the evaluation and solution of technical problems. Initiates the planning, organizing, performing, coordinating and/or directing of engineering work. Performs engineering studies. Remains abreast of and consults on technical advancements. Identifies and routinely uses the most effective, cost efficient and best practices to execute processes; continually evaluates their effectiveness and appropriateness.
Qualifications Requirements/Education: Bachelors Degree in Chemical/Mechanical Engineering, a related field, or equivalent experience. Typically a minimum of six plus years of progressively more responsible experience in the design, development and implementation of manufacturing processes and equipment as related to medical devices. Broad technical knowledge; expertise in one or more relevant specialties is also required. Demonstrated ability to develop new design features as part of existing systems. Requires comprehensive written and verbal communication, interpersonal, facilitation, presentation, quantitative, analytical, organizational, and follow-up skills, the ability to meet deadlines on multiple projects as well as the ability to converse effectively with all levels of employees. A documented record of delivering tool engineering information which adds value to managements decision making process is required. Demonstrated ability to understand and comply with applicable FDA regulations and Company operating procedures, processes, policies, and tasks. Advanced personal computer skills including spreadsheet, word processing database management, and specialized applications. Must be able to handle multiple assignments. Must be able to perform in a diverse cross-functional team environment. Desired Requirements: An advanced credential in a relevant discipline/concentration. Professional certification or designation. Six-Sigma knowledge and experience. Training and experience in manufacturing processes and methods. Experience in the manufacturing of medical devices. Academic or in-house courses in project management, Six-Sigma , leadership, training, TQM, and various technical applications as noted above are also desired.
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