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Polymer Processing and Manufacturing Engineer Nushores

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Polymer Processing and Manufacturing Engineer Nushores Polymer Processing and Manufacturing Engineer NuShores’ mission is to improve the quality of life for people globally while competing successfully by applying its licensed and internally developed advanced materials portfolio to the Biomaterials industry. NuShores has exclusive global license to patented bone and tissue regeneration technologies developed at University of Arkansas – Little Rock from over $12M in research. We are seeking a Polymer Processing and Manufacturing Engineer to Join our growing team to launch NuCress™ scaffold product family, our award-winning bone void filler line of medical device products. If working with a smart and creative team that designs and builds products that improve quality of life interests you, then consider a career with us. Job Type. Full-time professional employee. Reports To. The Polymer Process and Manufacturing Engineer will report to Chief Technical Officer, Chief Scientist or Product Manager. Salary. Competitive, with benefits. Job Overview. The Polymer Processing and Manufacturing Engineer will be the technical lead for new and existing processes that involve the integration of polymeric biomaterials to biological systems and products such as artificial bone and tissue medical devices. This role is responsible for concept development, equipment design and installation, vendor management, and process development and optimization for small to large-scale manufacturing readiness. A key focus for the Polymer Processing and Manufacturing Engineer is to lead process engineering to create and maintain a manufacturing line/facility. Additionally he/she will provide technical subject matter expertise in polymer structure-property relationships, catalyst, polymerization and to develop and maintain know-how and intellectual property within their relevant area of expertise to support regulatory and business objectives and sustain future growth. This engineering professional will work within a cross-functional team that includes scientists, regulatory experts, operations, proJect management, and business development to transition products from prototype stage to commercial launch. Responsibilities and Duties. § Provide team leadership as polymer processing subject matter expert within cross-functional project teams through all phases of product development process, including feasibility, process validation, and product launch. Primary duties will be on process engineering of a polymer- based product for quality manufacturing of medical devices. § Hands-on design and development of polymer processes and manufacturing equipment to meet business obJectives for product development. § Develop system specifications, test plans, protocols, and reports for designs, including biocompatibility and safety. Develop documents, specifications, protocols, production procedures, batch records, work instructions and test procedures. § Lead development of solutions to manufacturing challenges based on experimental data and implement those recommendations. § Develop and protect intellectual property associated with product or processes within area of expertise. § Maintain compliance to applicable regulatory requirements and internal quality policies. § Engage with proJect teams to assess proof-of-concept to support project execution (including design reviews and technology challenge sessions). § Develop and maintain vendor relationships including contracting for specific services and solutions with outside vendors, consultants, contractors, etc. Qualifications. § MS or PhD degree in Materials Science, Polymer Engineering, Chemical Engineering, Biomedical Engineering or related field, with a minimum of 5+ years industry experience. § Demonstrated ability to develop products and processes using a broad knowledge base in polymer engineering and processing, polymer characterization, and product performance testing especially in Medical Devices. Experience with current Good Manufacturing Processes (cGMP) validation and verification requirements of the FDA is a plus. § Working knowledge of ISO, ASTM, GDP, cGMP, and design controls is highly desirable. (especially ISO 13485) § Excellent organizational, written, and verbal communication skills is an essential requirement. § Ability to plan and execute innovative, multi-disciplinary product development projects within predefined specifications, budgets and deadlines. § Experience in processing biomaterials, especially biocompatible polymers is a plus. § Demonstrated track record of developing materials from concept to commercialization, preferably for medical devices is an asset. § Ability to Juggle multiple responsibilities and deadlines while communicating progress. § Ability to work independently and exercise appropriate Judgment under general direction. § Previous work at a startup is a plus. Work Authorization. proof of legal right to work in the US will be required of all candidates. Location. NuShores Biosciences is located in Little Rock, Arkansas, a city of momentum and energy with strong institutions like Fortune 500 companies, urban universities and technical colleges, hospitals, arts, historic museums and civil rights organizations. At the heart of the Natural State, Little Rock offers all the perks of an urban mid-size city with easy escapes to the bountiful surrounding nature (and its many biking and hiking trails, water sports, and outdoor adventures). Due to our solid economy, low cost of living and general quality of life, Little Rock is constantly featured in many quality-of-life lists from reputable magazines and blogs. We love it here, and we know you will too. Find out more at littlerock.com To apply, submit resume at www.nushores.com or email at [email protected]. .
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