Junior Systems Engineer

DEKA Research and Development, located in Manchester, NH, has an immediate opening for a Junior Systems Engineer to work in the Regenerative Medicine group. You will join a team that is developing electromechanical systems that monitor, control, and manipulate biologic materials to enable the manufacturing and deployment of cell-based therapies and tissue production. Systems Engineering is a high-visibility role with a significant, direct impact on the success of the project.How you will make an impact:Work with a small, fast-paced groupTranslate explicit and implicit stakeholder needs into actionable design requirementsDefine critical system features and subsystems interfaces in sophisticated software, electrical, mechanical, and biological systemsConduct research and engineering testing to guide product development and system integrationPerform risk management activities including: hazards identification, failure modes and effects analysis, risk analysis, root cause analysis, and risk benefits assessmentsAssist in the identification and evaluation of hazard mitigationsTroubleshoot failures, analyze data, take part in system design review meetings, and provide feedback to the development teamParticipate in brainstorming sessions on automation concepts, contributing interdisciplinary solutions to complex problemsHelp to ensure an overall level of product quality in line with DEKA’s quality and industry regulatory standardsTo be successful in this role, you will need the following skills and experience:MS/BS in Biomedical or Mechanical Engineering1+ years experience in an electromechanical role (Must show examples of multi-disciplined experience)Demonstrated problem solving ability and techniquesAbility to work as part of an interdisciplinary teamAbility to function as an individual contributor with minimal directionKnowledge and deep understanding of engineering fundamentalsPassion for biomedical technologies and problem solving using first principles thinkingExcellent verbal and written communication skills, detail orientedCell culture lab experience and knowledge of common tissue engineering strategies a plusExperience in medical devices, knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred

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