• Director US Labeling…

    Bayer (St. Louis, MO)
    ** Director US Labeling & Registration ** The Director US Labeling & Registration is responsible for the creation and maintenance of local ... The primary responsibilities of this role, Director US Labeling & Registration , are...contact information below. Bayer is an E-Verify Employer. **Location:** United States : New Jersey : Whippany… more
    Bayer (10/02/25)
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  • Senior Director , Clinical Leader…

    J&J Family of Companies (Titusville, NJ)
    …Job Posting Locations:** Allschwil, Switzerland, Beerse, Antwerp, Belgium, Cambridge, Massachusetts, United States of America, San Diego, California, United ... health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are... States of America, Titusville, New Jersey, United States of America **Job Description:** At… more
    J&J Family of Companies (09/03/25)
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  • Director , Regulatory Affairs

    Sumitomo Pharma (Tallahassee, FL)
    …I-IV Research & Development Activities + As a Regional Regulatory Lead, manage regional ( United States and/or European) regulatory activities as part of a Global ... company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma Canada,...highly motivated, and experienced individual for the position of ** Director Regulatory Affairs** . The Director is… more
    Sumitomo Pharma (09/09/25)
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  • Associate Director , Patient-Centered…

    AbbVie (Waltham, MA)
    …leads/participates in regulatory and reimbursement discussions and negotiations to optimize registration approval, product labeling & promotion and patient ... our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn… more
    AbbVie (09/17/25)
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  • Director , Environmental Operations

    Motrex LLC (Alpharetta, GA)
    …Element Resources (elementrellc.com) is one of the largest battery recycling companies in the United States . Recycling recovers 99% of all lead received at our ... (eg, universal waste, solid waste, and hazardous waste); waste generation registration and notification requirements; waste determinations; 90 day storage … more
    Motrex LLC (09/30/25)
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  • Sr. Director - Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    …better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to develop and ... business priorities in terms of the program's value proposition, workflow, product labeling , risk management, and issues management. Accordingly, the GRL is the… more
    Lilly (09/02/25)
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  • Senior Director Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    …better for people around the world. **Purpose:** The purpose of the Senior Director , Global Regulatory Affairs, Global Regulatory Lead (GRL) role is to develop and ... business priorities in terms of the program's value proposition, workflow, product labeling , risk management, and issues management. Accordingly, the GRL is the… more
    Lilly (09/03/25)
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  • Associate Director Regulatory Affairs

    Abbott (San Diego, CA)
    …role is part of the RA New Product Introduction (NPI) team, reporting to the Director of Global NPI and US Regulatory Affairs. We're empowering smarter medical ... will ensure data is identified, obtained, and effectively presented for product registration worldwide ( US , FDA, CE-IVDR, PMDA, etc.). **Strategic Planning:** +… more
    Abbott (09/12/25)
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  • Director , Regulatory Affairs

    BeOne Medicines (San Mateo, CA)
    …business partners regarding development, regulatory, and registration strategies within the US and Canada. The Director will also provide line management, ... **General Description:** The Director , Regulatory Affairs will be responsible for developing,...and submission of documentation to support investigational and marketing registration packages within the US and Canada… more
    BeOne Medicines (09/06/25)
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  • Sr. Director - Counsel, Cell & Gene Therapy

    Lilly (Indianapolis, IN)
    …a combination of the two + Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or ... companies, including, but not limited to: global product development, registration , and commercialization; FDA labeling and advertising requirements;… more
    Lilly (09/26/25)
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