Description The Life Science Innovation group at Client Technologies and Innovation in seeking a highly talented engineer to develop innovative solutions that address current and future health care needs in the area of infectious disease diagnostics. The associate will work as a member of a multidisciplinary team that is developing technologies to address the global infectious disease diagnostics market. The associate will develop build and test microfluidic devices and related components for biological sample purification. The associate will evaluate designs for manufacturability and contribute to the transition from prototype to validation devices and assembly procedures. Responsibilities will also include development of test methods and fixtures to characterize systems to determine release criteria and support validation. This position is a one year temporary position. The candidate will have an advanced set of skills and knowledge in device design for manufacturability fabrication and characterization and should be able to plan and conduct scientific experiments and effectively analyze interpret and present experimental results with minimal oversight. The candidate should also be able to adapt to changing requirements that can arise in a dynamic work environment and will be expected to contribute intellectually in areas not directly related to his or her field.
Responsibilities Design implementation and testing of microfluidic and/or electro-mechanical systems Develop tests and fixtures to evaluate performance and develop release criteria for microfluidic and/or electro-mechanical systems Transition prototype designs and assembly procedures to validation level devices and procedures Conduct device performance test with biological samples Review and provide input into acceptance criteria for technical specifications Communicate progress results conclusions and test steps to team and management Keep lab notes data and experimental observation in lab book Demonstrate strong personal accountability for completion of project milestones and deliverables Work independently receiving technical guidance on complex problems and supervisory approval on proposed plans for projects
Qualifications: BS or greater in Biology Biomedical Engineering Mechanical Engineering or related degree. 3-5 years of medical device experience. Experience with disposable microfluidic devices strongly preferred Experience with material selection device assembly injection molding machining practices and electro-mechanical assemblies. Experience in manufacturing process development validations and qualifications. Experience designing automated or semi-automated system tests is preferred. Experience with 3D CAD and Drafting (preferably SolidWorks Modeling). Proficiency with equipment/fixture fabrication and machine shop skills Self-motivation focus determination self-reliance open-mindedness amiability and flexibility Ability to work effectively within the project team and the cross-functional organization Working knowledge with biological samples and BSL2 environment a plus
Required Experience:
Contract
Job Title - Engineering ContractorLocation - Research Triangle Park NCDuration 12 Months ContractTotal Hours/week - 40.001st ShiftDescriptionThe Life Science Innovation group at Client Technologies and Innovation in seeking a highly talented engineer to develop innovative solutions that address cur...
Job Title - Engineering Contractor
Location - Research Triangle Park NC
Duration 12 Months Contract
Total Hours/week - 40.00 1st Shift
Description The Life Science Innovation group at Client Technologies and Innovation in seeking a highly talented engineer to develop innovative solutions that address current and future health care needs in the area of infectious disease diagnostics. The associate will work as a member of a multidisciplinary team that is developing technologies to address the global infectious disease diagnostics market. The associate will develop build and test microfluidic devices and related components for biological sample purification. The associate will evaluate designs for manufacturability and contribute to the transition from prototype to validation devices and assembly procedures. Responsibilities will also include development of test methods and fixtures to characterize systems to determine release criteria and support validation. This position is a one year temporary position. The candidate will have an advanced set of skills and knowledge in device design for manufacturability fabrication and characterization and should be able to plan and conduct scientific experiments and effectively analyze interpret and present experimental results with minimal oversight. The candidate should also be able to adapt to changing requirements that can arise in a dynamic work environment and will be expected to contribute intellectually in areas not directly related to his or her field.
Responsibilities Design implementation and testing of microfluidic and/or electro-mechanical systems Develop tests and fixtures to evaluate performance and develop release criteria for microfluidic and/or electro-mechanical systems Transition prototype designs and assembly procedures to validation level devices and procedures Conduct device performance test with biological samples Review and provide input into acceptance criteria for technical specifications Communicate progress results conclusions and test steps to team and management Keep lab notes data and experimental observation in lab book Demonstrate strong personal accountability for completion of project milestones and deliverables Work independently receiving technical guidance on complex problems and supervisory approval on proposed plans for projects
Qualifications: BS or greater in Biology Biomedical Engineering Mechanical Engineering or related degree. 3-5 years of medical device experience. Experience with disposable microfluidic devices strongly preferred Experience with material selection device assembly injection molding machining practices and electro-mechanical assemblies. Experience in manufacturing process development validations and qualifications. Experience designing automated or semi-automated system tests is preferred. Experience with 3D CAD and Drafting (preferably SolidWorks Modeling). Proficiency with equipment/fixture fabrication and machine shop skills Self-motivation focus determination self-reliance open-mindedness amiability and flexibility Ability to work effectively within the project team and the cross-functional organization Working knowledge with biological samples and BSL2 environment a plus