• Senior Project Manager - Global Medical Affairs

    United Therapeutics (Research Triangle Park, NC)
    …are as follows:** Who We Are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (09/04/25)
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  • Manufacturing Scientist II (Technology Transfer)

    ThermoFisher Scientific (Greenville, NC)
    …Lead projects with a moderate level of supervision, implement change control actions, review and plans technical aspects of the project to meet timeline and project ... operations, change controls, investigations as subject matter expert (SME). + Collects data for statistical analysis. Can support interpretation and summary of … more
    ThermoFisher Scientific (09/02/25)
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  • Senior Oncology Clinical Development Physician

    Astellas Pharma (Northbrook, IL)
    …of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We ... early-phase programs, safety management on trials, provides clinical input and review of clinical documents, statistical analysis plans, interim and final analyses… more
    Astellas Pharma (08/08/25)
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  • Global Insights & Demand Forecast Lead

    Takeda Pharmaceuticals (Bannockburn, IL)
    …Global Insights and Demand Forecast. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a value-led ... such as Regions) + Lead cross-functional teams in the review of demand forecast, epidemiology and its growth assumptions...to the organization + Serve as an SME on data and systems pertaining to sales performance (eg IQVIA… more
    Takeda Pharmaceuticals (08/02/25)
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  • Marketing Manager - Solutions Marketing

    BioFire Diagnostics, LLC. (Chicago, IL)
    The Marketing Manager for Pharmaceutical Solutions Marketing is responsible for executing targeted marketing strategies to drive business growth for our ... Pharmaceutical Quality Control (PQC) franchise in North America. This...Collaborate with Supply chain and sales administrators/sales managers to review forecasts of current and new products to ensure… more
    BioFire Diagnostics, LLC. (07/22/25)
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  • Clinical Pharmacist

    The County of Los Angeles (Los Angeles, CA)
    …monitors the effects of drug therapy using clinical symptoms, evaluating laboratory data , and other relevant clinical diagnostic techniques. Attends daily rounds and ... drug information services for healthcare providers and patients,including developing pharmaceutical newsletters, patient education materials, and assessment and evaluation… more
    The County of Los Angeles (07/19/25)
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  • Director, Regulatory Advertising & Promotion

    Sumitomo Pharma (Madison, WI)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... and mentoring. **Job Duties and Responsibilities** Advertising & Promotion Review Activities + Review and approve materials...+ 8 - 12 years experience in biotech or pharmaceutical industry with minimum of 8 years focused in… more
    Sumitomo Pharma (07/08/25)
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  • Senior Scientist, II

    AbbVie (North Chicago, IL)
    …and tracking, and periodical updates to management. + Independently design experiments, review data and complete results interpretation and reporting. Prepare ... and pipeline small molecule development within Science and Technology, Pharmaceutical Product Group. Key Responsibilities Include: + Lead analytical...and review documents for regulatory submissions. + Leading the analytical… more
    AbbVie (09/20/25)
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  • Senior Analyst, QA Stability (Pharmaceuticals)

    Contract Pharmacal Corp (Hauppauge, NY)
    …and storage conditions. Approve related protocols as applicable. + Write and/or review related Standard Operating Procedures. Approve such SOPs as applicable. + ... Write and/or review Deviation Reports related to the stability program. +...to the stability program. + Analyze and interpret stability data and documenting results in compliance with regulatory standards.… more
    Contract Pharmacal Corp (09/11/25)
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  • Validation Analyst II

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... regulatory requirements. + Author and execute test scripts, accurately document validation data , and compile final reports to support qualification and release of… more
    Curia (08/08/25)
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