Position Title
Product Development and Sustaining Engineer
SBU
Corporate
Department
Engineering
Relocation Covered
YES
Educational Requirements
Master's degree
Experience Requirements
A minimum of 5 years experience working in the design and development of medical devices and respiratory care products, along with experience in design and development of plastic injection molded components preferred. Interested internal applicants should forward an updated resume to Dalena Bobmanuel at: dbobmanuel@teleflexmedical.com. Ref# C194.
Qualification Requirements
Demonstrate creativity and ingenuity in applying engineering principles and practices. Draw solutions form a wider range of experience. Effectively present information and respond to questions from groups of managers, clients, customers, and the general public. Solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists; interprets a variety of instructions furnished in written, oral, diagram, or schedule form. Organize, evaluate, and coordinate engineering studies with professional, technical, and clerical staff of a product evaluation department. Analyze complex, technical and administrative problems and adopt an effective course of action. Conduct comprehensive studies and preparation of reports including recommendations. Make effective presentations to, and participate in a variety of meetings and conferences with other companies and the public. Establish and maintain cooperative relationships with those contacted in the course of work. Prepare clear and concise statements and reports. Establish and maintain cooperative relations with those contracted in the workplace. Speak and write English fluently.
Preferred Qualifications
Possession of Bachelors of Science degree mandatory. Possession of Masters of Science degree in engineering or closely related field preferred. Years of work experience in the design and/or modification of plastic components for the medical industry may be considered in lieu of Bachelors degree on an individual basis.
CADD (design/drafting) program, to include AutoCAD and SolidWorks Experience Microsoft Office Suite, (Project, Word, Excel and Access) Injection molding, plastic extrusion and plastic part assembly process and methods. U.S. FDA GMP and ISO requirements for the design, validation, manufacturing processes, secondary operations and assembly of medical components and devices. ISO and ASTM testing methods for medical devices and general plastic components Principles and practices of professional engineering. Regulations pertaining to medical device design and design modifications.
Responsibilities
This position is responsible for the development of new and maintenance of existing respiratory, anesthesia or urological products. Provides project mgmt for multiple projects and insures projects are completed in a timely manner within budget. Creates design ideas for new products as well as creative solutions to existing products when problems arise or modifications are requested. Performs other related duties as required.
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