The objective of the NIH Mentored Patient-Oriented Research Career Development Award (K23) program is to provide salary and research support for a sustained period of "protected time" (3-5 years) to ensure a future cadre of well-trained scientists conducting Patient-Oriented Research (POR). You should be able to self-direct, and take on ownership for your work, Proactive leadership skills, and the ability to identify design opportunities that can impact the business. Execution of the scientific method. and how they fit into the product development cycle for medical devices, Enrollment in a Bachelor degree program with an emphasis in Mechanical, Plastics or Biomedical Engineering, Completion of sophomore year of undergraduate schooling or greater, Strong analytical, fact-finding and problem-solving skills, Hands-on mechanical, laboratory, and/or testing skills, Support the engineering team in developing consumable medical devices, Perform preliminary designs, analyses and prototype/product bench testing, Gain experience in early product development, Assist in conceptual design with capture of intellectual property (as appropriate. as part of the assigned projects, May work in several departments to assist with completing any additional projects or tasks. Proactively bring new ideas and innovation to the Chocolate LA business, Relevant experience in R&D packaging or other relevant functions in Fast Moving Consume Goods Companies, expert in one or more areas, Proven knowledge in managing and developing people, Minimum of Bachelor Science in packaging, mechanical engineering, chemical engineering or materials science based. This is exactly where a career goals statement comes in handy. May supervise temporary and permanent lab technicians in the execution of assigned tasks. Change jobs. Your job usually involves determining the specific components of substances and in what quantity. What's best for you probably depends on the purpose of the resume. Ability to manage multiple tasks and have a sense of prioritization based on value and efficiency. Depending on the industry, a position in research and development has different educational requirements. Document work in a timely fashion in data books, internal reports. One needs to be very clear about his/her background. to anticipate future new product development needs, Develops and maintains strong collaborative development partnerships with other companies, academic institutions, opinion leaders and key customers, Provides technical and business leadership in the development of system products within a highly competitive diagnostics market. Non-degreed with 10+ years of relevant experience, Ability to initiate and complete analytical testing according to applicable standard operating procedures, in a routine service or research laboratory environment, within a defined timeline, Able to work under time pressure, sense of urgency and accuracy, Excellent knowledge and understanding of technical aspects of molecular biology related to DNA isolation, PCR and Real time PCR, Self-organization, planning, reporting and communication skills Computer skills including Windows 7, and MS Office, Previous experience with plants or agricultural crops preferred, but not required, Working safely in a Research and Development Technologist (R&D) environment, actively participating in company safety programs and implements improved Environmental Health & Safety practices, Work well both independently and on project teams in the spirit of advancing team and organizational goals, Communicates results and progress to technical team and supervision. of drafts and revisions of research/grant proposals, book proposals and presentation of research results in publications, Develop and deliver professional development materials and presentations that support the career growth and on-going needs of faculty. Obtain a position at ABC company as a Business Development Manager in order to use degree in computer science and skills involving the implementation of market research. Generating and maintaining documentation for the safe and efficient operation of equipment, Ability to troubleshoot equipment issues when encountered to accelerate repair, Interacting in a professional manner with the Business R&D teams, the Automation Group (Information Research), external equipment vendors and researchers within Formulation Science, Training new and existing personnel on equipment, The Dow Chemical Company does not offer relocation if the position is offered to someone who lives outside the area or reimbursement for travel to and from interviews. Skilled in presenting clear messaging to large audiences (>50 people), Supporting R&D Engineers throughout the design and development process, Brainstorming and evaluating concepts to bring an idea to new product development designs, Applying mechanical principals to the design and development of components for the Delivery Systems, Implants and/or accessory devices, Building prototype devices for design evaluation and concept selection, Performing accurate measurement and testing techniques utilizing calipers, micrometers, microscopes, rulers, optical comparators, vision systems, video comparators, tensile testing systems (Instron), inspection tooling and fixtures, Assisting in developing test methods and procedures to evaluate device prototype performances and developing specifications to evaluate device performance against design requirements, Performing feasibility testing to develop and verify device function, Training manufacturing assemblers and assisting in developing Manufacturing build procedures and in design for manufacturability, Performing Design verification testing and assisting in other engineering tests and animal studies, Maintaining accurate documentation of concepts, designs, drawings, and procedures with good documentation practices, Remaining up to date with training to TMVR Quality System requirements, and in compliance with safety policies and procedures with Lab Equipment and Testing, Ensuring that equipment used for R&D testing is appropriately calibrated and maintained, Supporting manufacturing and operational activities, including: manufacturing processes, tooling, training and troubleshooting, Interfacing with R&D Engineers and other technicians, Manufacturing, and Quality, to ensure compliance with internal procedures and Protocols, Familiarity with viewing, reading, and potentially creating parts/assemblies using Solidworks and/or Creo2 (ProE) and releasing design drawings into the Quality System, Facilitates Risk Management process in compliance to company policies and procedures. Resourceful & Growth trends. Strong rigour in record keeping and data compilation. Strong understanding and commitment to their own and the safety of others, Understanding of science and technology practices including the scientific method, and where potential divergences from expectations might be patentable discoveries, Proficient at developing and presenting data, Must have strong multi-tasking, problem solving and time management skills.A self-starter who can identify, prioritize and accomplish multiple tasks. Support capital plan assuring projects are completed successfully, on time, and within approved budgets, Foster team environment through development/implementation of improved work practices, Provide leadership, direction, planning and execution of Pilot Plant Operations and Materials Management area activities per established R&D business unit priorities, The Supervisor is accountable to the Operations Manager for controlling budget, payroll and capital of at least $3MM, The Supervisor responsibility impacts all nutritional products produced in the plant and the preservation of the company’s continued well-being through compliance to regulations and avoidance of major business interruptions from regulatory agencies such as the FDA, This position is responsible for ensuring proper equipment/manpower utilization, good employee relations, a safe environment, quality products and profitability, Strategy for the clinical development of medicines, Integration and incorporation of all early clinical development work including biomarkers and companion diagnostics, Timelines and budget for clinical development of medicines, Design and conduct of all clinical trials of medicines globally (including Asia and Japan), Alignment with Regulatory Affairs, Global Project Leadership, Research & Early Development/translational medicine as well as Market Access, Medical Affairs and commercial functions, Lead the CR&D Therapeutic Area team, attract, retain and develop talent for all roles in the team, be responsible for engagement and collaboration across the team, Drive indication and product strategic vision through strong scientific and medical knowledge, exceptional understanding of the drug development process and a strong ability to contribute/lead cross-functional teams, Active membership of the cross-functional Oncology Leadership Meeting (OLM) and the department-internal CR&D Leadership Team, Active membership and functional leadership in the cross-functional Disease Strategy Team for MDS/AML, ability to lead such a team, Incorporate a sound business sense into the clinical development program, Very close collaboration and partnership with Regulatory Affairs to drive clinical strategic objectives, submissions and approvals, Medical/clinical review on due diligence and in-licensing opportunities, Build efficiency and innovation into the clinical development program and look for innovative ways to do clinical trials - like biomarker strategy, Understand how all clinical development groups work together and how it all funnels into clinical data flow, Take a role within the global CR&D leadership team in order to advance the work of the whole department, Organize and lead advisory boards and investigator meetings relevant to clinical projects with the respective teams in the therapeutic area, Responsible as a thought leader in the development of new and innovative strategies related to regulatory and clinical use of new and existent pharmaceuticals, Responsible for clinical budget allocations, capacity planning and responsibility for utilization reporting and budget review and tracking, Develop strong and reliable relationship to Celgene’s partners in the joint development of medicines for this therapeutic area, A solid background in all phases of clinical development which includes, Basic laboratory skills, including liquid handling, reagent preparation, and chemistry-related calculations- including calculations of stock concentrations, making serial dilutions, etc, Execution of high-throughput screening experiments, Bachelor’s or Master’s degree in the life sciences or physical sciences, Independent undergraduate research experience, 0-2 years of experience at a pharmaceutical / biotechnology company or research institute, Outstanding written and oral communication skill, Capable of multitasking and properly prioritizing tasks, Experience with basic Microsoft Office programs (Excel, Word, etc, Experience in pharmacology, enzymology, or assay development, Planning, reviewing and financial reporting of the assigned R&D Operating Plan and budget, primary focus on Avelumab alliance, Understanding and determining the impact of latest business dynamics for the, R&D function(s); focus on Avelumab alliance, Directly responsible for maintaining the appropriate environment of internal financial controls in all aspects of the Avelumab alliance, Developing and preparing decision support models, business cases and, Presentations that support the management decision making, Drives financial planning and budgeting for relevant R&D functions and/or projects and provide input to strategic planning from early to late stage development, Collaborates with business partners to integrate corporate and divisional targets into operating plan, Develops and prepares analysis, decision support models, and business cases, Assists the Senior Corporate, Divisional and US Management, on a wide range of ad hoc requests, Promoting "best practice" approach, suggesting and driving further, Improvements of existing reporting and processes, Advising operational business with respect to financial benefits and risks of, Acquisition targets and/or strategic partnerships, particularly Avelumab alliance, Takes a continuous improvement attitude to communicate/ share relevant information with team members to ensure best practices and consistency across the various functions, Excellent English, written, oral, negotiations, Minimum required 5 years’ experience related to the area of Financial Analysis/Planning / Controlling in the pharmaceutical industry, Experience with drug discovery and development, Expertise of SAP, MS office excel and powerpoint, International Travel of up to 20% working time on annual basis required for this position required, Personal network of industry and academic leaders in assistive / rehabilitative human neurotechnology, Experience leading a long-range, advanced R&D program toward applied outcomes, Experience in implantable or non-invasive neural sensing, recording, imaging, data analysis, stimulation or modulation, Experience leading and directing experiments in a clinical setting, Experience developing business strategies, Minimum 10 years experience in automotive design and development, Prior management experience strongly desired, Experience using Spacevision and/or any 3D software, Excellent Presentation/communication skills, Demonstrated history for taking proactive approach, Self-motivated, assertive, learner, fair, transparent and remains calm in the face of multiple stressful situation, Candidates for this position must be legally authorized to work in the United States and will be required to provide proof of employment eligibility at the time of hire. Track productivity, address gaps, and communicate to stakeholders, Identifies patent opportunities to improve Mondelēz International’s competitive advantage in the marketplace, Lead ideation sessions to identify programs, complete scoping and initiate development activity, Lead and influence ingredient gum base programs to benefit the G&C Category, Unleash the power of people by providing challenging experiences that grow and develop people. Closely monitors non-standard work requests and reviews with management prior to initiation, Assigns and conducts testing of products in accordance with supplied procedures. Your research manuals and job aids, logs maintenance activities and calibration results required. Progress to commercialization and implementation consistent with project needs and handles multiple tasks in parallel, strong leadership to. Via weekly status reports and white papers you can find a job in almost any industry candidate be... 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