LinkedIn - Jobboard
R&D Test Engineer [Entry Level]
LinkedIn - Jobboard, Franklin Lakes, New Jersey, us, 07417
Position: R&D Test Engineer [Entry Level]
Location: Franklin Lakes, NJ
Duration: 12+ Months Contract
Total Hours/week: 40.00
1st Shift
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
No H1B’s
Description
For the hardware tester position, it has to be local FLKS site. For testing, needs to be in lab every week day.
The R&D test engineer position is an entry level position, responsible for hardware testing activities to develop and commercialize complex instrumentation in the medication safety space.
The R&D test engineer will support engineering studies and Design Verification activities for the Intelliport products including disposable sensors and several reusable electro-mechanical devices. In addition to testing, this associate may also contribute to the improvement of testing methods, measurement system development & analysis of test methods, the improvement of fixtures, data processing and analysis. The testing performed in this role will help ensure that our products meet our customer’s expectations and regulatory requirements. Knowledge of disciplined product development processes, regulatory, quality requirements and design controls, such as 21 CFR 820.30 is a plus.
Minimum Qualifications
Bachelor’s degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering, Applied Physics or similarProficient in reading and understanding assembly drawings, manufacturing and test instructions, and service manuals.
Desired Qualifications
Experience testing medical device product for Design VerificationKnowledge on testing software, firmware and hardware by following test protocolsWorking knowledge of regulatory standards applicable to design of medical devices, including FDA QSR, ISO 13845, ISO 14971 and IEC 60601 and collateral standardsPost-educational experience in Medical Device DesignDesign for Six Sigma, Design for Manufacturability and Reliability training / experienceGraduate degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering or Applied PhysicsFluent in CAD modeling such as Solidworks or ProE
Competencies
Excellent written & verbal communication skillsSelf-directed with the ability to learn and adapt quickly to new technologies and trendsStrong organization and coordination skillsAbility to work independently after appropriate directionCareful, deliberate, disciplined, meticulous, and well organized in performing laboratory tests and recording resultsAbility to read and follow Standard Operation Procedures, Good laboratories Practices, Good Documentation Practices knowledge
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Location: Franklin Lakes, NJ
Duration: 12+ Months Contract
Total Hours/week: 40.00
1st Shift
Client: Medical Device Company
Employment Type: Contract on W2 (Need US Citizens Or GC Holders Only)
No H1B’s
Description
For the hardware tester position, it has to be local FLKS site. For testing, needs to be in lab every week day.
The R&D test engineer position is an entry level position, responsible for hardware testing activities to develop and commercialize complex instrumentation in the medication safety space.
The R&D test engineer will support engineering studies and Design Verification activities for the Intelliport products including disposable sensors and several reusable electro-mechanical devices. In addition to testing, this associate may also contribute to the improvement of testing methods, measurement system development & analysis of test methods, the improvement of fixtures, data processing and analysis. The testing performed in this role will help ensure that our products meet our customer’s expectations and regulatory requirements. Knowledge of disciplined product development processes, regulatory, quality requirements and design controls, such as 21 CFR 820.30 is a plus.
Minimum Qualifications
Bachelor’s degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering, Applied Physics or similarProficient in reading and understanding assembly drawings, manufacturing and test instructions, and service manuals.
Desired Qualifications
Experience testing medical device product for Design VerificationKnowledge on testing software, firmware and hardware by following test protocolsWorking knowledge of regulatory standards applicable to design of medical devices, including FDA QSR, ISO 13845, ISO 14971 and IEC 60601 and collateral standardsPost-educational experience in Medical Device DesignDesign for Six Sigma, Design for Manufacturability and Reliability training / experienceGraduate degree in Mechanical Engineering, Systems Engineering, Biomedical Engineering or Applied PhysicsFluent in CAD modeling such as Solidworks or ProE
Competencies
Excellent written & verbal communication skillsSelf-directed with the ability to learn and adapt quickly to new technologies and trendsStrong organization and coordination skillsAbility to work independently after appropriate directionCareful, deliberate, disciplined, meticulous, and well organized in performing laboratory tests and recording resultsAbility to read and follow Standard Operation Procedures, Good laboratories Practices, Good Documentation Practices knowledge
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