3D Systems Validation Support Engineer - 180000RR in Littleton, Colorado

About 3D Systems Colorado3D Systems Colorado is a dynamic and leading enterprise, specialized in 3DPrinting of metal components. 3D Systems Colorado is not only a technologydeveloper but also a technology user. This makes us a strong innovationpartner for clients in the industrial, medical, aerospace and dental sectors.With this technology, we build up material in layers using a high intensitylaser until it becomes a solid product. Unlike conventional productiontechniques, this one does not render any material loss, nor does itrequire any tooling. It does however, enable the designers to manufacturevery complex geometries which are not producible using the traditionaltechniquJOB DESCRIPTION Our site in Littleton Colorado is looking for a top notchengineer to support the manufacturing of products in the high tech,aerospace and healthcare industries using 3D Systems' platforms.The Validation Support Engineer is responsible for focusing interfacing withcustomers to help facilitate the implementation of process controls andvalidations as regulated by the ISO 13485, ISO 9001, AS9100 and globalrequirements such as FDA QSR, MDD and various aerospace regulations. Thisposition is responsible for supporting the development and execution ofmanufacturing processes and quality systems in accordance with internalguidelines as well as customer driven requirements.In this job, you will not only cooperate with your service and applicationengineering colleagues world-wide but you can also rely on the knowledge andexperience of colleagues from other 3D Systems divisions.RESPONSIBILITIESCollaboration with project teams, including both internal and externalstakeholders, as a contributing member by providing quality and processengineering support in the development of new products and processes using 3DSystems' products. Application development of new technologies to enhancethe capabilities of 3D Systems' Contributing to the development andexecution of verification & validation plans, testing, and generation oftest protocols and reports Development and contribution to the risk managementprocess Development and contribution of process controls and planningParticipating in the compilation and review of technical documentation forboth domestic and international regulatory submissions Assisting project teamson compliance with design control requirements per FDA QSR, European MDD,ISO 13485/9001 and other applicable ISO/EN standards Participating in theexecution, maintenance and improvement of the Quality Management System.PROFILEBachelor degree, preferably in engineering. Masters preferred2-4 years of related work experience in regulated, cGMP environment such asmedical device, pharmaceutical or food manufacture.Quality assurance and reliability experience supporting product developmentand/or manufacturing are preferred.Working knowledge of GMP and ISO 13485 Quality System preferredAbility to read and design engineering specifications across a number ofproducts and materials.Ability to analyze and develop engineering processes for use in advancedtechnology implementations.Fluent in EnglishVEVRAA Federal ContractorRequest Priority Protected Veteran ReferralsEqual Opportunity Employer-minorities/females/veterans/individualswith disabilities/sexual orientation/gender identity