• Associate Director - Life Sciences Advisory…

    Guidehouse (Boston, MA)
    …program design, implementation, and monitoring services to pharmaceutical, biotechnology, and medical device , companies. We support our clients across the ... multiple projects simultaneously of all varying sizes and durations to ensure quality control and key client's perceived value while supervising, mentoring and… more
    Guidehouse (08/18/25)
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  • Senior Deposition Processes Execution Lead

    RTX Corporation (Andover, MA)
    …issues as well as the ability to work with operations, facilities, equipment, and quality teams. The role requires a large degree of multitasking with attention to ... interact with various process engineering, equipment engineering, digital technologies, quality , facilities, and operation teams **Qualifications You Must Have:** +… more
    RTX Corporation (09/06/25)
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  • Semiconductor Backside Via Process Lead

    RTX Corporation (Andover, MA)
    …issues as well as the ability to work with operations, facilities, equipment, and quality teams. The role requires a large degree of multitasking with attention to ... interact with various process engineering, equipment engineering, digital technologies, quality , facilities, and operation teams **Qualifications You Must Have:** +… more
    RTX Corporation (08/14/25)
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  • Lead Microbiology Technician

    Integra LifeSciences (Braintree, MA)
    …preferred. + 5+ years GMP/GLP laboratory experience in a medical device , pharmaceuticals, Quality /Regulatory Compliance , or other regulated industry + ... procedures. + Support the implementation of new or improved quality control systems as needed. + Ensure compliance... quality control systems as needed. + Ensure compliance with industry regulations, company policies, and safety standards… more
    Integra LifeSciences (08/08/25)
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  • Associate Program Manager, Access & Affordability…

    IQVIA (Northborough, MA)
    …what it takes to deliver nationally and internationally. Our teams help biopharma, medical device and diagnostic companies get their therapies to the people ... patients or prescribers. With the right experience, you can help deliver medical breakthroughs in the real world. The Associate Program Manager is responsible… more
    IQVIA (09/05/25)
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  • Operations Supervisor

    BD (Becton, Dickinson and Company) (Woburn, MA)
    …Mechanical Engineering or related field + Minimum of 2 years experience in a medical device manufacturing environment or related industry + Ability to work ... procedures and Quality System Regulations and supervise day to day compliance of department personnel. + Support an environment of open communication and… more
    BD (Becton, Dickinson and Company) (09/07/25)
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  • Manager, Analytics & Data Engineering, Onsite

    AbbVie (Worcester, MA)
    …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 ... Analytics and Data Integrity to lead site analytics web and data quality initiatives within our pharmaceutical operation reporting into Digital Systems organization.… more
    AbbVie (07/12/25)
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  • Senior Manager-Corrections & Removals

    Philips (Cambridge, MA)
    …of Post Market Surveillance/C&R teams, detailed knowledge in FDA and Global Medical Device regulations, strong communication and collaboration skills, with a ... important role in ensuring Sleep & Respiratory Care product quality and patient safety. **Your role:** + Will Manage...regulatory inquiry responses, and reviews these responses to ensure compliance with C&R standards. + Leads meetings with senior… more
    Philips (09/04/25)
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  • Final Inspector I

    Neotech (Westborough, MA)
    …to all ESD requirements and Board Handling. + Use of Moisture Sensitive Device (MSD) handling requirements based on component moisture sensitive levels (MSL). + ... Verify product compliance to workmanship standards. + Verify process ...and follow all ISO standards related to OnCore's various Quality Management Systems. These systems may include, but are… more
    Neotech (07/04/25)
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  • Senior Technical Clinical Consultant (PACS,…

    Fujifilm (Boston, MA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... for project and or post go-live support cases in compliance with the company's quality procedures. **Company...+ Ability to work effectively with customers in the medical field. + Ability to prioritize and handle multiple… more
    Fujifilm (06/19/25)
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