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C. R. Bard, Inc. (NYSE: BCR) is a leading multinational developer, manufacturer and marketer of innovative, life-enhancing medical technologies in the fields of vascular, urology, oncology and surgical specialty products, employing over 11,000 people in over 25 countries around the world. Founded more than 100 years ago, we pioneered many devices that are now the cornerstones of modern healthcare.
We expect the highest levels of quality, integrity, service, and innovation from our employees – on the job and in the communities in which we work and live. In return, we foster an environment where individuals are treated with fairness and respect, and feel valued, acknowledged and rewarded.
Be Your Best at Bard – and ultimately, you can have an impact on the lives of people around the world.
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| Overview: |
The Sr. Project Engineer position is located in Covington, GA. at Bard Medical Division.
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| Summary of Position with General Responsibilities: |
This position is responsible for new product discovery, research and development, and project management for products at Bard Medical Division. The Pelvic Health product group develops unique solutions for treating various pelvic floor disorders, including incontinence and pelvic organ prolapse. Products include both surgical implants and handheld delivery systems for the minimally-invasive treatment of these conditions. This position involves working with physicians to develop new and less-invasive products and procedures to deliver the next generation of urological and gynecological healthcare to patients
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| Essential Job Functions: |
Responsible for leading programs and generating new product concepts directed toward new commerical products and/or unique, functionally superior modifications of existing products Involved in all aspects of the porduct development cycle beginning with concept generation and prototyping, then moving into production and product release. Involved in multidisciplinary responsibilities including product conceptualization and design to meet end user requirements. Serves as a creative/technical resource to other sectors within the division. Responsible for evaluating and identifying project and product risks. Use technical training to relate diverse technologies and to understand novel concepts/solutions of problems that may be abstract and only semi-defined. Develops, manages, and maintains project timelines from concept through developmenet and qualificaiton using Microsoft Project or other equivalent software. Interfaces with a wide variety of specialty disciplines. Generates and/or evaluates several new product concepts per year with expectation that some will be proprietary and perhaps patentable. May be responsible for supervision and development of direct reports.
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| Basic Qualifications: |
• Demonstrated track record of project and team leadership in a fast-paced product development environment
• Foundation and experience in medical product design, including some 3-D CAD experience (SolidWorks preferred)
• Working knowledge of design control, FDA regulations, and ISO standards for medical devices
• Strong interpersonal skills required in the areas of verbal and written communications, customer focus, professionalism, coaching, and team building
• Strong questioning and problem-solving skills
• Experience with prototyping techniques (e.g., SLA, machining, RTV molding, etc) and various manufacturing processes (e.g., injection molding, machining, plastic and metal processing, assembly techniques, etc)
• Proficient in the use of software programs such as MS Word, Excel, PowerPoint, Outlook, and Project, or equivalent programs
• Experience with handheld mechanical devices and implantable biomaterials is preferred
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| Additional Desirable Qualifications Skills and Knowledge: |
Ability to read and comprehend technical documents/essays and write technical reports. Ability to perform standard engineering calculations. Knowledge of Statgraphics a plus.
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| Education and/or Experience: |
BS in Mechanidal, Bio-Medical or Industrial Engineering 8+ years experience in new product/process development in medical device industry Prior supervisory experience
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| Physical Demands: |
May be required to sit, bend, stoop, use keyboard, see, talk and hear. May occasionally lift objects of 10 to 25 lbs. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.
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| Work Environment: |
Normal office environment. Noise level is quiet to moderate.
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