• Manager, Regulatory Affairs

    Bio-Techne (Minneapolis, MN)
    … professionals, working closely with the Sr. Director , Regulatory Affairs and the R&D Systems (RDS) Quality Assurance team to ensure compliance ... unique portfolio of products and services. POSITION SUMMARY The Regulatory Affairs Manager at R&D Systems will...primarily achieved through project team membership. + Partner with Quality Assurance team to provide general regulatory more
    Bio-Techne (09/26/24)
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  • Senior Director Global Regulatory

    Danaher Corporation (Minneapolis, MN)
    Affairs department and report to the Vice President of Global Quality and Regulatory Affairs . The Director of Global Regulatory Affairs will ... of solutions that safeguard and improve human health. This position is part of Quality and Regulatory Affairs located in Fargo, ND and will be fully remote.… more
    Danaher Corporation (10/02/24)
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  • Principal Regulatory Affairs

    Philips (Plymouth, MN)
    …clinical study approvals and review of clinical study protocols. + Reporting to the Director of Regulatory Affairs -Ultrasound, you will partner with ... The Principal Regulatory Affairs Specialist will play a...mentor/coach Philips regulatory professionals; drive improvement in regulatory aspects of the Quality Management System,… more
    Philips (08/27/24)
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  • Executive Director , Device Quality

    Merck (St. Paul, MN)
    …processes. + Stay updated on emerging regulations and industry trends affecting device quality and regulatory affairs . Strategic Contributions + Serve as ... **Job Description** The Executive Director , Device Quality & Regulatory...and Skills:** + 10+ years of experience in device quality , device regulatory affairs , or… more
    Merck (10/24/24)
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  • Senior Manager, Clinical Affairs US

    Danaher Corporation (New Brighton, MN)
    …in Bronshoj (Denmark) and the US Hub in Minneapolis. This position will report to the Director of Clinical Affairs in the US and will be based in New Brighton, ... address the world's biggest health challenges. The Sr. Clinical Affairs Manager is responsible for directly managing a team...play a critical role in the timely, effective, and quality completion of clinical studies. This position is responsible… more
    Danaher Corporation (09/07/24)
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  • Director , Principal Scientist Device…

    Merck (St. Paul, MN)
    …of Position-** This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The ... the collection and analysis of data for management review. **Reports to** - Director Regulatory Compliance, Device Quality and Regulatory **Location** -… more
    Merck (10/25/24)
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  • Director , Regulatory & Customer…

    Post Holdings Inc. (Hopkins, MN)
    …walk or outdoor lunch before, within, or after your work day. Responsibilities The Director of Regulatory Affairs and Customer Compliance is responsible for ... **Brand:** Michael Foods Inc. **Categories:** Quality **Locations:** Hopkins, Minnesota **Position Type:** Regular Full-Time...overseeing and providing leadership for all regulatory and export compliance matters within the MFI Integrated… more
    Post Holdings Inc. (09/05/24)
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  • Business Development Director

    Cardinal Health (St. Paul, MN)
    …of capacities, including: + Global Regulatory Strategy Development + Global Regulatory Affairs + Chemistry Manufacturing and Controls (CMC) Development + ... selling to Pharmaceutical, Biotech and Medical Device companies client preferred. + Regulatory affairs , drug development understanding is highly preferred. +… more
    Cardinal Health (10/04/24)
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  • Associate Director , Global Labeling Lead…

    Takeda Pharmaceuticals (St. Paul, MN)
    regulatory nuances and requirements. + Knowledge of scientific principles and regulatory / quality systems relevant to drug development. + Ability to create, ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
    Takeda Pharmaceuticals (10/16/24)
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  • Global Medical Director , Allergy

    ThermoFisher Scientific (Minneapolis, MN)
    …your medical knowledge to assist different departments, such as marketing, sales, manufacturing, quality and regulatory affairs . You will also collaborate ... challenging work, and join a team that values performance, quality and innovation. As part of a successful, growing...experienced individual to join our team as Global Medical Director , Allergy on the Medical and Scientific Affairs more
    ThermoFisher Scientific (09/27/24)
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  • Contract Center Medical Director /Center…

    CSL Plasma (Minneapolis, MN)
    …Staff Associates for completion of training and recommendation for certification by Regulatory Affairs . Functionally directs the Center Medical Staff. Provides ... as or delegates to another appropriate physician the duties of "laboratory director ", "technical consultant", or "clinical consultant" as prescribed by the Clinical… more
    CSL Plasma (10/14/24)
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  • Director , Global Strategic Marketing

    Teleflex (Maple Grove, MN)
    Director , Global Strategic Marketing **Date:** Oct 9, 2024 **Location:** Maple Grove, MN, US **Company:** Teleflex **Expected Travel** : Up to 25% **Requisition ID** ... driven by our purpose to improve the health and quality of people's lives. Through our vision to become...make a difference in patients' lives. **Position Summary** The Director of Global Strategic Marketing will lead, manage, and… more
    Teleflex (09/11/24)
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  • Executive Director

    Brookdale Senior Living (West St. Paul, MN)
    …resident and resident family engagement and connection, financial performance, and regulatory compliance. Creates and executes the business plan and develops the ... drive sales results. Creates an inclusive community culture that provides high quality resident experiences and care and engages residents, families, and associates.… more
    Brookdale Senior Living (11/01/24)
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  • Associate Director Project Management Oligo…

    WuXi AppTec (St. Paul, MN)
    …in TIDES drug development from discovery through clinical to commercial. Moreover, our Regulatory Affairs CMC team is experienced in preparing CMC dossiers to ... WuXi STA. WuXi TIDES offers our worldwide partners efficient, flexible, and high- quality solutions for the drug development of oligonucleotides, peptides and related… more
    WuXi AppTec (10/18/24)
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  • Senior Audit Manager - Corporate Functions

    US Bank (Minneapolis, MN)
    …Function - Other is a management position that supports the Corporate Functions, Regulatory Reporting, and SOX Administration Audit Director . This role supports ... the Audit Director and Senior Audit Director , in providing the Audit Committee and senior management...responsible for auditing various areas within Strategy and Corporate Affairs . Specific areas of audit responsibility include M&A, DEI,… more
    US Bank (09/06/24)
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  • Principal Clinical Scientist - Maple Grove, MN St.…

    Abbott (St. Paul, MN)
    …trials from concept to execution by working collaboratively with biostatistics, medical affairs , regulatory affairs , global clinical operations, and other ... including clinical project management, clinical operations, clinical science, biostatistics data management, regulatory affairs , medical affairs as well as… more
    Abbott (10/31/24)
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  • Clinical Research Manager - Structural Heart

    Medtronic (Mounds View, MN)
    …be assigned. + Provides leadership for the conduct of clinical studies and for the regulatory affairs function as it applies to product approval. + Studies must ... from key functional groups (Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs , and European Clinical Groups) to drive clinical… more
    Medtronic (08/17/24)
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  • Senior Clinical Project Manager

    ZOLL Medical Corporation (Minnetonka, MN)
    …on the status of trial conduct to the Chief Medical Officer and Director of Clinical Affairs . Required/Preferred Education and Experience + Bachelor's Degree ... normal breathing pattern during sleep and give them better quality of life. We develop breakthrough therapies for an...+ Review and approve monitoring reports. + Train Clinical Affairs team members on the clinical investigational plan, the… more
    ZOLL Medical Corporation (10/08/24)
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  • Stability Chemist III

    Actalent (Minneapolis, MN)
    …+ Collaborate with vital team members such as Product Design Owners, Project Managers, Regulatory Affairs , and Quality to anticipate business needs and gain ... and makes recommendations that are non-routine to address technical, regulatory , and business requirements. Responsibilities + Represent R&D-Stability on project… more
    Actalent (11/03/24)
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  • Physician Clinical Reviewer- GI- Remote

    Prime Therapeutics (St. Paul, MN)
    …determinations with requesting physicians or ordering providers, when available, within the regulatory time frame of the request by phone or fax. + Provides ... training per inter-rater reliability process. + Assists the VP, Medical Affairs in research activities/questions related to the Utilization Management process,… more
    Prime Therapeutics (09/21/24)
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