• Lundbeck (Deerfield, IL)
    …years of Compliance-related experience in the healthcare industry (ie. pharmaceutical, medical device , biologics, healthcare or consulting company that supports ... years Compliance-related experience in in the life sciences, pharmaceutical, biotech or medical device industry. This may include consulting experience or… more
    DirectEmployers Association (11/13/25)
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  • Medical Director , Medical

    AbbVie (North Chicago, IL)
    …Headquarters) and open to other AbbVie office locations in the US. Purpose: Medical Device Safety Physician leads the safety oversight relevant to her/his ... clinical safety input to new product design teams as needed. The Medical Device Safety Physician is independently responsible for proactive safety strategy, … more
    AbbVie (10/26/25)
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  • Sr Director - Device Assembly…

    Lilly (Pleasant Prairie, WI)
    …who are determined to make life better for people around the world. The Device Assembly and Packaging (DAP) Operations Sr Director is responsible to provide ... to the DAP Flow Team for the Lilly Kenosha site. The Operations Director will deliver the operational organization and readiness agenda in alignment with the… more
    Lilly (09/01/25)
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  • Associate Director , Quality Control…

    Lilly (Pleasant Prairie, WI)
    …manufacturing investments and new state of the art QC laboratories. The Associate Director , Quality Control (QC) - Chemistry, is responsible for leading the site QC ... organization, specifically operations relating to Chemistry Testing, Device Testing, Stability Administration, Laboratory Informatics and Instrumentation/Equipment Management.… more
    Lilly (11/01/25)
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  • Manager, Category Management - Drug Delivery…

    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 ... . Job Description Purpose The Category Manager - Drug Delivery Device leads implementation of category procurement strategy, developed in partnership with… more
    AbbVie (11/06/25)
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  • Director , Medical Affairs

    Abbott (Abbott Park, IL)
    medical specialist dedicated to all medical aspects of safe and effective device heart failure treatment. The director will report to the Chief Medical ... external regulatory agencies and professional societies. WHAT YOU'LL WORK ON: The Medical Director o Develops medical opinions, medical platform… more
    Abbott (09/18/25)
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  • Senior Director , Medical Affairs

    Abbott (Abbott Park, IL)
    …and scientists **The Opportunity** We are seeking a highly experienced and strategic Senior Director of Medical Affairs to lead medical and scientific ... / TriClip. + Strong knowledge of cardiovascular anatomy, physiology, pharmacology, and device interactions. + Skilled in medical monitoring, adverse event… more
    Abbott (10/11/25)
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  • Associate Medical Director

    AbbVie (North Chicago, IL)
    …potentially leading one or more products as the PSTL under the direction of the Group Medical Director and Executive Medical Director in ensuring safety ... Leads and implements risk management strategy for assigned products Key Stakeholders: Group Medical Director , Executive Director , TA Head, PST Lead,… more
    AbbVie (09/23/25)
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  • Medical Director

    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 ... surveillance. * Responsible for safety surveillance for pharmaceutical / biological / drug - device combination products * Lead, oversee, and set the strategy for key… more
    AbbVie (10/01/25)
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  • Associate Director , Global Supply Planning

    AbbVie (North Chicago, IL)
    …position is responsible for the operations and strategic design of the US Medical Device & Aesthetics businesses global supply planning organization which ... support very significant revenue streams for Medical Device & Aesthetics businesses. Achieving the revenue goals are critical to AbbVie's top line revenue goals… more
    AbbVie (10/21/25)
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  • Product Security Director

    Brunswick (Mettawa, IL)
    …Summary:** The Information Security Team at Brunswick is seeking an experienced Director of Product Security to lead our comprehensive product security strategy ... product leaders to execute a strategy that algins with business objectives, the Director of Product Security will seek to ensure effective security postures across… more
    Brunswick (10/12/25)
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  • Sr. Director , Market Access - Payer Value…

    Abbott (Abbott Park, IL)
    …access, payer strategy, and patient support services within the pharmaceutical, biotech, or medical device industries. The ideal candidate will bring a bold ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
    Abbott (10/25/25)
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  • Associate Director , Quality (Hybrid)

    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 ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director , Quality provides leadership and direction to the Quality Function… more
    AbbVie (11/15/25)
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  • Associate Director , Site Data Integrity…

    Lilly (Pleasant Prairie, WI)
    …computer science-related field preferred + Minimum 5 years working in the pharmaceutical or medical device industry in QA roles + Minimum 3 years of experience ... that impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will also provide computer system quality assurance oversight… more
    Lilly (09/10/25)
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  • Director , Quality & Regulatory Business…

    GE HealthCare (Arlington Heights, IL)
    …Qualifications** + Master's Degree and a minimum of 7 years' experience in the medical device or pharmaceutical industry; or Bachelor's Degree and a minimum of ... 9 years' experience in the medical device or pharmaceutical industry; or will consider a High School Diploma and a minimum of 13 years' of progressive… more
    GE HealthCare (08/26/25)
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  • Manufacturing, Engineering and Contracting (ME&C)…

    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 ... Engineering & Contracting (ME&C) team within Global Operations, the ME&C Strategy Director & Chief of Staff will directly support the Senior Vice President… more
    AbbVie (11/06/25)
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  • Associate Director , Global Quality…

    AbbVie (North Chicago, IL)
    …Quality Assurance, Regulatory, Operations, or Technical Support in a pharmaceutical or medical device setting required. Experience working in a regulatory agency ... 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… more
    AbbVie (11/15/25)
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  • Associate Director , Program Management…

    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 ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible for managing major… more
    AbbVie (09/30/25)
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  • Sr. Director , Parenteral Engineering

    Lilly (Pleasant Prairie, WI)
    …determined to make life better for people around the world. The Engineering Sr. Director - Parenteral Engineering role is a critical role to ensure we continue to ... with highly automated equipment + Previous experience with combination products, device assembly, pharmaceutical packaging, drug product formulation and filling in… more
    Lilly (09/24/25)
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  • Regulatory Affairs Specialist

    Danaher Corporation (Richmond, IL)
    …field or equivalent experience. + Minimum of two years' experience within medical device /IVD, across a variety of regulatory submissions, compliance initiatives, ... actions. + Experience with ISO 13485:2016, IVD/MDR Regulations, FDA GMP and domestic/international Medical Device Regulations. It would be a plus if you also… more
    Danaher Corporation (10/17/25)
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