Project Engineer

Position : Project Engineer Location : Holdrege, NE Duration : 9 Months contract Total Hours/week : 40.00 1st Shift Client: Medical Device Company Level Of Experience: Mid-Level Employment Type:Contract on W2 (Need US Citizens Or GC Holders Only) Hours: Mon through Fri ~8am to 5pm  Some flexibility if needed Job Description: General Function: Lead engineering projects to improve plant capabilities through new or improved processes, technology and equipment while also providing engineering and technical support. Essential Functions (Responsibilities): Essential functions include, but are not limited to, the following: Project Management Lead projects to reduce cost, increase efficiency, improve safety, or improve machine capabilities from conception through to completion Manage and coordinate project timelines, team meetings, project reviews, project budgets, equipment installations and validations Effectively communicate project requirements, goals and timelines to plant management Act as a vendor liaison for the purchase, design, fabrication, installation, and validation of custom high speed automation equipment Provide problem solving, cost analysis, testing, validation, design, and equipment repair support. Assist in writing capital requests and developing departmental budgets Engineering Support Brainstorm, research, design and test new processes, technologies and equipment Collaborate on equipment designs with outside vendors and other client engineers Produce CAD models and prints using AutoCAD, Inventor, and/or SolidWorks software Prepare comprehensive machine specifications for use in the fabrication and purchase of new equipment Create work instruction and quality documentation for new processes and equipment Provide engineering support for production through cost analysis, testing, equipment design, equipment repair and problem solving. Perform acceptance testing for newly purchased equipment General Work to promote a team atmosphere which fosters respect, open communication, and trust Communicate well with other engineers, floor associates, vendors, plant management, and the corporate office Demonstrate attention to detail in both designs and project management Position Requirements: Knowledge & Experience Education: Bachelor degree in Engineering, (BSME or BSEE preferred). Desired Experience: Application of QSR to new and modified operations / procedures. Minimum of two years of engineering experience in manufacturing (preferably medical device manufacturing). Equipment design experience. Desired Knowledge/Skills/Abilities: Demonstrated verbal & written communication skills. Strong problem solving skills. Demonstrated leadership skills. Working knowledge of manufacturing processes and technology. PC skills; familiarity with Excel, Word, PowerPoint Minitab, SAP, CAD, MS Project and Visio. Understand preventive maintenance concepts and management of work orders. Proficiency with 3D CAD software (preferably Inventor or Solidworks). Supervision: Indirect supervision over support personnel necessary for project completion including engineers, technicians, quality associates, facilities associates, and equipment operators. Other Functions (Responsibilities) May Not Be All Inclusive All requirements are subject to possible modification to reasonably accommodate individuals with disabilities. Some requirements may exclude individuals who pose a direct threat or significant risk to the health and safety of themselves or other associates. This job description in no way states or implies that these are the only duties to be performed by the employee occupying this position. Associates will be required to follow any other job-related instructions and to perform any other job-related duties requested by their supervisor. Requirements are representative of minimum levels of knowledge, skills and/or abilities. To perform this job successfully, the incumbent will possess the abilities or aptitudes to perform each duty successfully. Conditions of employment in this facility include, but are not limited to: Associates must obey all safety rules. Associates must follow all QSR (GMP) regulations. Associates must cooperate fully with the safety and environmental program. Associates may not pose a direct threat or significant risk to himself/herself or others. The "Essential Functions" and "Other Functions" listed in this description do not restrict the addition or deletion of any other responsibilities to this position. Management reserves the right to change any and all job descriptions without notice as business conditions dictate. All associates are expected to know and adhere to the Becton Dickinson Core Values which are: We treat each other with respect. We do what is right. We always seek to improve. We accept personal responsibility. About Client: Client, a leading global medical technology company that makes and sells medical devices, instrumented systems and reagents, is dedicated to improving people's health throughout the world. The Company's capabilities are instrumental in combating many of the world's most pressing diseases. Founded in 1897 and headquartered in Franklin Lakes, New Jersey, Client employs more than 25,000 people in approximately 50 countries throughout the world. The Company serves healthcare institutions, life science researchers, clinical laboratories, industry and the general public. It was one of the first companies to sell U.S.-made glass syringes. It was also a pioneer in the production of hypodermic needles and ranked #195 in the 2019 Fortune 500 list. It was also listed among the top 100 companies in Newsweek's 2009 Green Rankings. Ranking of the 500 largest American corporations based on environmental performance, policies, and reputation. Placed third in the health care sector and 83rd overall