• Quality Systems Engineer

    Jabil (Auburn Hills, MI)
    …auditor or advanced knowledge of Regulatory and ISO standards (Automotive, Telecom, Medical Device , or other industry QMS/EMS standards). + Strong working ... of the site's critical Quality System programs. You'll ensure compliance with regulatory requirements, lead cross-functional problem-solving initiatives, and provide… more
    Jabil (12/13/25)
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  • Clinical Research Manager

    Children's Mercy Kansas City (Kansas City, MO)
    …Manager OR Required Upon Hire + ACRP-MDP Assoc of Clinical Research Professionals - Medical Device Professional Required Upon Hire + If RN, refer to Nursing ... clinical research operations, including quality management, personnel management, regulatory compliance , as well as collaborating with Principal Investigators and… more
    Children's Mercy Kansas City (12/13/25)
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  • Jt510 - Sr EHS Specialist

    Quality Consulting Group (Juncos, PR)
    …Knowledge of OSHA, EPA, DOT, and local environmental regulations relevant to medical device manufacturing. + Experience conducting risk assessments, ergonomics ... QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and… more
    Quality Consulting Group (12/13/25)
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  • Quality Assurance Manager

    BD (Becton, Dickinson and Company) (El Paso, TX)
    …Minimum 7 years' experience in quality, with at least 3-5 years in the medical device industry or pharmaceutical industry. + Minimum 2-3 year's management ... Inspection, Final Product Release, Quality Engineering, Supplier Quality while maintaining full compliance with FDA Quality System Regulations (21 CFR Part 820), all… more
    BD (Becton, Dickinson and Company) (12/13/25)
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  • Sr. Maintenance Technician- 3rd shift

    Cardinal Health (Chicopee, MA)
    …a highly skilled and experienced **Senior** **Maintenance Technician** to support our medical device facility and production manufacturing operations. This role ... is critical to ensuring equipment reliability, reducing downtime, and maintaining compliance with FDA, ISO, and DEP standards and regulations. **Responsibilities:**… more
    Cardinal Health (12/12/25)
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  • Driver CDL/ Warehouse Associate

    Mondelez International (Fargo, ND)
    …the year based on needs. **R** **esponsibilities and duties:** + Ensuring compliance with procedures and conducting regular safety checks on warehouse equipment to ... performing order picking, palletizing, and loading/unloading delivery trucks. + Ensure compliance with procedures and regular safety checks of your equipment… more
    Mondelez International (12/12/25)
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  • Senior/Principal - Cloud Solutions Architect,…

    Sandia National Laboratories (Albuquerque, NM)
    …state or federal law. NNSA Requirements for MedPEDs: If you have a Medical Portable Electronic Device (MedPED), such as a pacemaker, defibrillator, ... of onsite work and working from home) + Generous vacation, strong medical and other benefits, competitive 401k, learning opportunities, relocation assistance and… more
    Sandia National Laboratories (12/12/25)
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  • Document Manager

    Insight Global (Pleasant Prairie, WI)
    compliance with regulatory requirements and internal quality standards for a medical device manufacturer. Key Responsibilities * Document Development & ... meet regulatory standards (FDA, ISO 13485) and internal quality requirements. * Compliance & Governance ○ Maintain document control systems in alignment with Good… more
    Insight Global (12/12/25)
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  • Marketing Manager

    Envista Holdings Corporation (Brea, CA)
    …+ 2+ years in downstream marketing or product management + Experience in medical device , dental, or infection prevention industries + Proven success in ... and legal teams to ensure marketing strategies align with healthcare compliance and product capabilities; translate clinical data into compelling marketing… more
    Envista Holdings Corporation (12/11/25)
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  • Quality Engineer 1 NPD

    J&J Family of Companies (Irvine, CA)
    …0- 2 years of quality, manufacturing, or research and development experience in a medical device or other regulated industry + Ability to define problems, ... design verification tests, process validations and quality processes to ensure compliance with the company's Quality System policies and procedures and applicable… more
    J&J Family of Companies (12/10/25)
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