• Quality Assurance Batch Release Associate…

    Lilly (Indianapolis, IN)
    …to make life better for people around the world. **Organization Overview:** Drug Product External Manufacturing - US (DPEM) Quality Assurance assures patients ... worldwide of safe and efficacious drug products, through effective quality oversight of North American contract manufacturers and alliance partners. This oversight… more
    Lilly (05/03/25)
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  • Registered Nurse RN Clinical Research Specialist

    Banner Health (Mesa, AZ)
    …to the clinical trial schedule, which may include: maintaining, dispensing and recording drug and medical device supplies according to regulations; assisting in ... **EEO Statement:** EEO/Female/Minority/Disability/Veterans (https://www.bannerhealth.com/careers/eeo) Our organization supports a drug -free work environment. **Privacy Policy:** Privacy Policy (https://www.bannerhealth.com/about/legal-notices/privacy)… more
    Banner Health (04/16/25)
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  • Clinical Research Associate II - Smidt Heart…

    Cedars-Sinai (Los Angeles, CA)
    …the development of Investigator Initiated trials for Investigational New Drug applications and/or Device applications **Qualifications** **Educational ... field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures,… more
    Cedars-Sinai (04/16/25)
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  • Registered Nurse RN Clinical Research Specialist…

    Banner Health (Sun City, AZ)
    …to the clinical trial schedule, which may include: maintaining, dispensing and recording drug and medical device supplies according to regulations; assisting in ... **EEO Statement:** EEO/Female/Minority/Disability/Veterans (https://www.bannerhealth.com/careers/eeo) Our organization supports a drug -free work environment. **Privacy Policy:** Privacy Policy (https://www.bannerhealth.com/about/legal-notices/privacy)… more
    Banner Health (03/15/25)
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  • Senior Global Marketing Manager, Hazardous…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …best self. Become a **maker of possible** with us. **Summary** The Hazardous Drug Solutions (HDS) platform is focused on protecting healthcare workers globally by ... Experience + 5+ years of experience in product management within medical device or related industry **Knowledge and Skills** + Understanding of pharmacy compounding… more
    BD (Becton, Dickinson and Company) (05/18/25)
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  • Medical & Scientific Affairs Clinical Liaison (CL)

    Fortive Corporation (Irvine, CA)
    …+ Knowledgeable of US Food and Drug Law and regulatory, drug safety and/or device vigilance and/or regulatory/clinical research requirements in major ... geographies. \#LI-RB **Fortive Corporation Overview** Fortive's essential technology makes the world stronger, safer, and smarter. We accelerate transformation across a broad range of applications including environmental, health and safety compliance,… more
    Fortive Corporation (04/29/25)
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  • Senior Staff Global Process Owner, Quality…

    Danaher Corporation (Brea, CA)
    …and federal environmental regulations and standards including compliance with Food & Drug Administration (FDA), Medical Device Single Audit Program (MDSAP), ... ISO13485, European Union Medical Device Directives (MDD), and In-Vitro Medical Device Regulation (IVDR) as well as all other applicable global regulatory… more
    Danaher Corporation (05/24/25)
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  • Deputy Director

    Public Citizen (Washington, DC)
    …the climate crisis, fair trade, consumer protection, access to justice, workplace safety, and drug and medical device safety. We are the reason why there are ... air bags and backup cameras in cars and why there were no red M&Ms for a decade. And much more. APPLICATION DEADLINE: March 21, 2025. Applications will be considered on a rolling basis, so please submit your materials quickly. RESPONSIBILITIES + Management:… more
    Public Citizen (05/20/25)
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  • Sr. Compliance Specialist

    Medtronic (Lafayette, CO)
    …BE ASSIGNED:** + Mastering knowledge of applicable Quality, FDA (Food & Drug Administration) Medical Device Directives/ Regulation, HIPPA (Healthcare Information ... Patient Privacy Act) and ISO (International Organization for Standardization) requirements through the updating of policies and procedures and acting as a liaison with appropriate policy experts. + ProvidesQuality System support and guidance tomaintain… more
    Medtronic (05/14/25)
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  • QMS Document Control Owner

    Danaher Corporation (Pensacola, FL)
    …document control management and product lifecycle management systems, in biotech, pharma, drug product, or medical device document control experience preferred + ... Strong foundational knowledge in current Good Manufacturing Practice (cGMP) and Good Documentation Practice (GDP) + Highly skilled in Microsoft Word for comparing and merging documents, creating and using templates, creating form using fields and using advance… more
    Danaher Corporation (05/07/25)
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