• Associate Director Regulatory

    Abbott (St. Paul, MN)
    …catheters and software, vessel closure devices and peripheral stents. **The Opportunity** This ** Associate Director Regulatory Affairs ** will work on-site at ... in the Vascular Division. As a manager, the function of an Associate Director Regulatory Affairs is to combine knowledge of scientific, regulatory more
    Abbott (03/20/24)
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  • Director Public Policy, State Affairs

    Humana (St. Paul, MN)
    …health first** The Director of State Public Policy role resides within the Corporate Affairs Department and will serve as an expert in state public payer, Medicaid ... businesses. The Director of State Public Policy role resides within the Corporate Affairs Department and will serve as an expert in state public payer, Medicaid… more
    Humana (02/15/24)
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  • Medical Instrument Technician (Echocardiography)

    Veterans Affairs, Veterans Health Administration (Minneapolis, MN)
    …for which he/she is responsible. Knowledge of JCAHO and other regulatory requirements. Ability to communicate effectively and professionally with employees at ... program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus...two years of education above high school or an associate 's degree with a major field of study directly… more
    Veterans Affairs, Veterans Health Administration (04/19/24)
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  • Medical Laboratory Aid/Medical Technician

    Veterans Affairs, Veterans Health Administration (Minneapolis, MN)
    …promoted to the full performance level without further competition when all regulatory , qualification, and performance requirements are met. Selection at a lower ... program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP) Participation in the Coronavirus...per week. OR Education: Successful completion of (a) an associate -degree course of study of which the 2nd year… more
    Veterans Affairs, Veterans Health Administration (01/31/24)
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  • Associate Director, Global Labeling

    Takeda Pharmaceuticals (St. Paul, MN)
    …You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met ... life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Global Labeling Lead where you will be...+ Acceptable and independent skills in the area of regulatory affairs such as understanding broad concepts… more
    Takeda Pharmaceuticals (03/29/24)
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  • Associate Director, GMP Quality Control

    Sumitomo Pharma (St. Paul, MN)
    …changes to contract manufacturing organizations, testing laboratories, clinical sites and regulatory affairs as needed. + Responsible for compliance with ... ** Associate Director, GMP Quality Control** Sumitomo Pharma America...ensures compliance with GMPs, SMPA procedures and applicable global Regulatory guidelines by providing oversight and management of the… more
    Sumitomo Pharma (04/19/24)
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  • Associate Account Manager

    Enviri Corporation (Blaine, MN)
    …or the ability to rapidly establish relationships within the C-level, Regulatory Affairs , Quality, Procurement, Supply Chain, Operations and Marketing ... to rapidly establish relationships within the Environmental Health and Safety, Regulatory Affairs , Quality, Procurement, Supply Chain, Operations and Marketing… more
    Enviri Corporation (04/24/24)
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  • Associate Director, Clinical Quality…

    Merck (St. Paul, MN)
    …colleagues, GCTO Country Operations, other GCTO functional areas, Pharmacovigilance (PV), Global Regulatory Affairs and Clinical Safety (GRACS), IT, etc.) is ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing… more
    Merck (04/24/24)
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  • Associate Clinical Research Manager (aCRM)…

    Merck (St. Paul, MN)
    …with HQ functions, regional and local operations, EU Clinical Development, Pharmacovigilance, Regulatory Affairs , Global Medical and Scientific Affairs to ... **Job Description** **Position Description:** ** Associate Clinical Research Manager (aCRM) - Oncology** With...the TA-Head or CRD. + Requires understanding of local regulatory environment. + Scientific and clinical research knowledge is… more
    Merck (04/26/24)
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  • ATQ Platform QC Sr Associate

    J&J Family of Companies (St. Paul, MN)
    …our production and testing processes. + Support Change management processes and work with regulatory affairs to understand and handle impact of Changes to the ... ATQ Platform QC Sr Associate - 2406182260W **Description** **"Caring for the world...is required. + Advanced knowledge in Change management and regulatory processes. + Analytical knowledge including knowledge about internal… more
    J&J Family of Companies (04/18/24)
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  • Region Associate Director / Region…

    Bristol Myers Squibb (Minneapolis, MN)
    …of Medical Strategies, Objectives and FM Plans within boundaries established by regulatory and legal compliance in accordance with company policies and sound ethical ... stakeholders (eg site leadership, thought leaders, scientists, research staff, pharmacists, industry- affairs office personnel, etc.) + Effective and timely triage of… more
    Bristol Myers Squibb (04/10/24)
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  • MSL/Sr MSL Enterprise Research, Oncology (Midwest)

    AbbVie (Minneapolis, MN)
    …patient or compassionate use basis, subject to all applicable legal and regulatory requirements. * Must provide insights on the current clinical practice, facilitate ... * Support Enterprise Critical Studies' related activities from a medical affairs perspective and contributing to meeting study timelines. * Provide scientific… more
    AbbVie (04/19/24)
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  • Contract Center Medical Director/Center Physician

    CSL Plasma (Minneapolis, MN)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... training to other center staff on medically related procedures and practices. 5. Reviews and signed Medical Staff Associates notebooks weekly, including a review of approximately one out of five screening medical evaluations and unsuitable test result… more
    CSL Plasma (04/16/24)
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