• DOLA Campus Program Specialist (Community…

    State of Colorado (CO)
    …location and great benefits, which include: + Medical and Dental Plans (https://dhr.colorado.gov/state-employees/state-of-colorado-employee-benefits) + Strong, ... HUD housing quality standards (HQS), as well as programmatic compliance and outcomes. Travel Requirements: Travel to Sage Ridge...to distracted driving or use of a mobile electronic device as described in CRS 42-4-239. + No convictions… more
    State of Colorado (12/10/25)
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  • Senior Equipment Calibration and Preventive…

    Cordis (Irvine, CA)
    …organized work approach. **Preferred:** + Experience in Class IIb or III implantable medical device manufacturing. + Previous experience in a cleanroom or ... the development of ground-breaking technology and commercialization of advanced drug device combination products for the treatment of coronary and peripheral artery… more
    Cordis (12/09/25)
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  • Quality Engineer -Sustaining Engineering (SE)

    PCI Pharma Services (Rockford, IL)
    …years of experience in an FDA regulated industry with strong preference to medical device or combination products. + Demonstrated proficiency with personal ... implementing validation strategies, conducting tests, and analyzing data to confirm compliance and functionality. The QVE will interact and collaborate with internal… more
    PCI Pharma Services (12/04/25)
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  • Exec Director, Regulatory Affairs-Combination…

    Gilead Sciences, Inc. (Washington, DC)
    …poster. NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT (http://www.dol.gov/whd/regs/ compliance /posters/eppac.pdf) YOUR RIGHTS UNDER THE FAMILY AND ... accelerate development and approval timelines. Provide guidance to PDM Teams and Device Teams to align development and regulatory path for combination products and… more
    Gilead Sciences, Inc. (12/03/25)
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  • Senior Principal Systems Engineer

    AbbVie (North Chicago, IL)
    …medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's ... will contribute to the development and launch of exciting new drug / device combination products. As a Sr. Principal Systems Engineer, you will be responsible… more
    AbbVie (12/03/25)
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  • Head of Service Intelligence

    Roche (Indianapolis, IN)
    …are:** _Required Qualifications:_ + Bachelor's degree + 8 years of experience in Diagnostics, Medical Device Industry and/or Life Sciences + 5 years of people ... analytics, or field service systems, including 5+ years in the medical device industry + Proven success leading data-driven service transformation in a… more
    Roche (12/03/25)
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  • Talent Acquisition Partner

    Permobil (Lebanon, TN)
    …for executing full-cycle recruiting to attract, engage, and hire top talent within our medical device manufacturing organization. This role plays a key part in ... 4-6 years of progressive experience in talent acquisition, preferably within manufacturing, medical device , or other regulated industries. + Strong understanding… more
    Permobil (12/02/25)
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  • Sr Teamcenter Technical Program Manager

    Cognizant (Dallas, TX)
    …the end-to-end development and implementation of Teamcenter PLM solutions within the medical device industry. This role requires strong leadership, technical ... Compliance & Quality: Ensure PLM solutions adhere to FDA, ISO, and other medical device regulatory standards. Roadmap Development: Define and execute the PLM… more
    Cognizant (12/02/25)
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  • Manufacturing Engineer II

    Stratasys (Belton, TX)
    …procedures to meet the standards and requirements of aerospace, automotive and medical device industry customers. Leveraging your expertise in manufacturing and ... (NRE) efforts + Understanding of key criteria and requirements of aerospace, medical device , and/or automotive industries + Experience applying Lean… more
    Stratasys (11/25/25)
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  • Quality Engineer, Design Control

    Hologic (San Diego, CA)
    …environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR 820, ISO 13485 as well as CE ... team member on New Product Development projects to ensure compliance with design controls, as well as identify and...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
    Hologic (11/21/25)
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