R and D Engineer - Stryker (lakeland, FL)

Job Title R and D Engineer Division Stryker Sustainability Solutions Business Unit U.S. Business Sub:Functions New Product R and D Country United States State FL City Lakeland Shift 1st Job Description The R and D Engineer designs, develops, and improves new processes for medical devices and directs the testing and evaluation of medical devices. DUTIES and RESPONSIBILITIES: ? Advanced understanding of project leadership skills needed to effectively lead a multiple tasked and cross functional team projects to completion. ? Advanced understanding of project management principles to effectively complete assignments and achieve desired outcomes. ? Increased project ownership and accountability ? Uses team management skills to lead the design group during product development through product launch ? Directs development of an action plan and estimates requirements for resources : management, tasks, budgets, labor, materials, and time required to complete projects. ? Monitors progress of development project and compares actual costs with estimates. ? Leads design team to modify plans as appropriate if problems arise. ? Prepares communication in weekly reports, status updates, detailing progress and costs for management. ? Discusses project status reports at monthly project reviews with executive team and design review meetings. ? Advanced ability to generate detailed project plans, multitask, and fast tracking of project tasks. ? Plans and directs new product development ? Ability to effectively interact within a team environment and with other departments such as Quality, Operations, Regulatory Affairs, Mfg. Engineering, Customer Service, Marketing, Sales, as well as external customers and suppliers. ? Establishes test protocols specified by customer input, national and international standards, and regulatory requirements. ? Directs and facilitates the testing of new products to verify product reliability. ? Interaction with production/manufacturing for design transfer to production floor ? Leads the development of technical protocols and reports. ? Improve/support existing processes. ? Advanced knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions. EDUCATION and EXPERIENCE: ? Bachelors degree in an engineering or science field. ? 1:3 years of practical experience in the medical device industry or 5+ years exp. in medical device industry plus advanced degree. (medical device company preferred) ? Advanced understanding of Statistical Methods and Project Management Principles (formal training preferred) ? In:depth knowledge of medical terminology/concepts related to medical devices. ? Knowledge of FDA requirements associated with the development of medical devices including Design Control and the technical support required for regulatory submissions. ? Proficient in managing projects and project management principles to effectively complete assignments and achieve desired outcomes. ? Proficient in project management, ownership and team member supervisory skills. ? Excellent organizational skills and ability to plan/prioritize activities. ? Ability to work independently or with a team. ? Strong verbal and written communication skills; ability to present issues, plans and objectives. ? Ability to work in fast paced organization, meeting multiple deadlines and succeeding under pressure is a must. ? Motivated, resourceful, ambitious, enthusiastic and attentive to detail. ? Proficient in Microsoft Word, Excel, Power Point, Outlook, Project, Visio ? Exposure Source:

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