R&D Design Engineer Job
Location: Somerville New Jersey
Description: Johnson & Johnson is hiring R&D Design Engineer Job right now, this position will be placed in New Jersey. More details about this position opportunity please give attention to these descriptions. Johnson & Johnson companies are equal opportunity employers.
R&D Design Engineer-8312131202
Description
Ethicon Biosurgery, a member of the Global Surgery Group within the Johnson & Johnson's Family of Companies, is currently recruiting for a R&D Engineer, located in Somerville, NJ.
The Global Surgery Group is comprised of the following businesses within Johnson & Johnson: Ethicon Surgical Care, Ethicon Energy, Ethicon Biosurgery, Acclarent, Biosense Webster, Cordis, Mentor and Sterilmed. With annual sales of $11 billion, the Global Surgery Group is ! the world’s largest, most innovative surgical company. The s! trength of the Global Surgery Group is illustrated by the fact that more than 80% of our sales come from businesses with #1 or #2 global market share positions. We serve customers around the world, with about 60% of our sales generated outside the U.S., including a fast-growing presence in emerging markets. The Global Surgery Group is committed to innovation, with about 30% of our sales coming from products introduced in the past five years.
Our R&D team of scientists, engineers, and technical experts are in the forefront of technology, working in the complex world of combined drug / device based medical products. You will be making a vital contribution to the New Product Development pipeline and transforming patient care. Our Design Engineers execute specific & general assignments/projects that provide innovative, functional, cost effective & validated product designs in a team based environment.
Key Responsibilities include:
Apply knowledge of! general engineering principles, materials, DFMA & reliability to achieve product design requirements.
Work one-on-one with customer stakeholders to identify procedure and/or product opportunities and evaluate potential technical solutions.
Interpret customer & marketing input to define technical design requirements, utilizing QFD (quality function & deployment), JOC (jobs, outcomes, & constraints), VOC (voice of customer) methodologies & surgical procedure knowledge to define product & design options.
Provide innovative product, system, & component design solutions while coordinating the integration of complex sub-system product designs.
Perform detailed design analysis & provide input or approval for detailed design specifications.
Develop free-body diagrams, develop transfer functions, calculate stress & strain values, and formulate tolerance stack-ups.
Establish appropriate testing strategy to insure adequate safety ! factors or margins. Perform product testing to insure adequate safety f! actors or margins.
Document engineering tests and reports, technical documents, and design related work in a concise, focused, and thorough means.
Formalize concepts, breadboards & prototyping.
Aid in the creation, generation, development, and refinement of intellectual property while providing support to patent attorneys for patent filing.
Assist in developing & monitoring project plan, budget, contingency plans & work estimation.
Provide technical leadership to product development team.
Learn and implement knowledge of medical terminology, procedures & instrumentation to create innovative design solutions.
Provide peer feedback & mentor junior associates as required.
Have a passion for your work and a sincere interest to improve patient outcomes.
Qualifications
In this position, a BS degree (preferably Mechanical Engineering), with a minimum of 3 + years of design-related experience ! is required (preferably in medical products or device industry working in a cross functional environment is preferred). Working on a design team is preferred. Regulated industry is required.
Core mechanical engineering skills required, including free-body diagraming, stress-strain analysis, FEA (finite element analysis), and stack-up analysis.
Prefer knowledge of geometric dimensioning & tolerance (GD&T) and Gage repeatability & reproducibility (GR&R).
Knowledge of general manufacturing engineering and DFMA principles is an asset, including component manufacturing processes, tooling / equipment methodologies are required, and material properties is required.
Experience with3-D solid-modeling, and 2-D printing is required.
Experience with statistical analysis techniques (DOE, Capability Analysis, SPC) are an asset.
Outstanding leadership capabilities with the innate talent to work in a cross-functional team environment.
Networking and the ability to communicate with outside sources ! is requirement.
Basic knowledge & understanding of medical regulatory requirements. Experience working in a clinical based project environment is a plus.
Technical writing experience: protocols, testing results, procedures, status & special reports is required.
Project management and leadership skills is an asset.
Information & risk analysis skills is an asset.
Negotiation (e.g., internal & external customers) and conflict analysis / resolution is required.
Ability to provide review of designs and provide constructive feedback to fellow engineers and scientists is required.
Able to adapt to shifting priorities, handle a rapid pace environment, and to resolve problems / conflicts.
Able to take initiative & be self-managing is required.
It is required to travel up to 20% both domestic and international.
BE VITAL in your career; Be seen for the talent you bring to your work. Explor! e opportunities within the Johnson & Johnson Family of Companies.
J2W: LI
Primary Location: North America-United States-New Jersey-Somerville
Organization: Ethicon Inc. (6045)
Job : R&D Engineering (R&D)
Relocation: Eligible Yes - Within Country
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If you were eligible to this position, please email us your resume, with salary requirements and a resume to Johnson & Johnson.
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This position starts available on: Fri, 06 Dec 2013 17:30:4! 7 GMT