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Solid foundation of using material characterization techniques needed for understanding materials interaction with device performance:STEM, EDS, SIMS, PL, XRD, CV, Eddy Current, XPS, etc. Previous direct or indirect experience with physical semiconductor device modeling techniques.
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Contribute to development and conduct of scientific studies (benchtop, in vitro, ex vivo, and/or in vivo) to characterize concept device performance. The candidate will be responsible for providing mechanical and biomaterials engineering support through the development and testing of medical device design solutions and materials interfacing with tissue and drug formulations.
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Baebies is a medical device company that develops and commercializes newborn screening and near-patient testing products for children and adults to enable early disease detection and comprehensive diagnosis.
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Complete maintenance, device repairs, and services including Smokes, VESDA, NAC Panels, A/Vs, Pull Stations, Fire Extinguishers, Sprinkler systems, PIVs, Hydrants, etc. Knowledge of Fire Protection and Fire Alarm systems including VESDA, Hazard Fire Suppression Systems, Sprinkler Systems, and Fire Alarm and Detection Devices.
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Knowledge of wafer processes and basic device processing, with a good background in thin film deposition, dry/wet etch, or photolithography. Hands-on engineering resource for fabricating IR emitter pixels on test and device wafers.
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Assisting with traffic control device installation and flagging operations for stationary and moving work zones. Assisting with asphalt, concrete, stormwater and street cleaning operations and/or projects.
$39,141 - $57,953 a yearExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Our research is used by pharmaceutical, biotechnology, medical device/diagnostic, and other healthcare technology manufacturers and Health Technology Assessment authorities worldwide to inform their decisions about the availability, pricing, and reimbursement of new healthcare interventions.
$75,000 - $95,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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A minimum of 6 years' experience in pharmaceutical, medical, device, biotech, or clinical trial contract research industry, including minimum 2 years' experience in Quality Assurance and/or Regulatory Compliance/Affairs.
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One to three years test engineering experience in an electro-mechanical device development environment. Support device testing and execution under direction of senior team members. Education in data analysis techniques (e.g., tests for means/variance, categorical analysis, Gauge R/R) with data analysis tools (JMP, Minitab, Excel, MATLAB, or others.
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In addition, you have 2+ years of experience working in clinical data management, clinical or lab research, and/or related work experience in a medical device or pharmaceutical industry/company.
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The scope of the role includes syringe filling and device assembly & packaging operations for commercially manufactured products targeted for transfer to the RTP site. Our company is designing and building a new state of the art Parenteral, Device Assembly, and Packaging Facility located at the Research Triangle Park (RTP) in North Carolina.
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Knowledge of other regulatory, compliance, and legal issues related to health care including (1) FDA Regulations (and other international equivalents); (2) ICH-GxP requirements; (3) global medical device and in vitro diagnostic registration requirements; (4) transparency laws; and (5) human biological specimen regulations.
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IND), Investigational Device Exemption (IDE), Institutional Review Board (IRB. Advanced degree (MSc, PhD) in biomedical engineering, sciences, health outcomes research, or related field preferred.
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MCSE and other Infra certificationsStrong Architecture Design skillsStrong Cloud device configuration experienceExperience with Vmware, Azure and containerizationAbility to work on-call or non-standard business hours as neededNOTE: This role may require additional duties and/or assignments as designated by management.
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Candidates may need to be qualified for work under Exec Order 14042, Vaccine Mandate for workers on federal contractsCompetencies (as demonstrated through experience, training, and/or testing)Must be able to meet and continue to meet any applicable state, county and municipal licensing and permit requirements for armed security work and specific protective device and weapons qualifications.
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device job in Durham, NC
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