• Director , Computational Multiomics,…

    J&J Family of Companies (Spring House, PA)
    …of internal and external human data resources. + Partner with Clinical Development, Global Regulatory Affairs , Data Science, Patient Reported Outcomes, ... while championing patients every step of the way. We are searching for a ** Director , Computational Multiomics, Neuroscience,** to be located at one of our offices in… more
    J&J Family of Companies (11/18/25)
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  • Senior Director - Quality Assurance Head,…

    Gilead Sciences, Inc. (Foster City, CA)
    …digital tools and analytics per our **Quality digital roadmaps** **Compliance & Regulatory Affairs ** + Ensure site-wide compliance with cGMP, FDA, EMA, ... Gilead and help create possible, together. **Job Description** The Senior Director , Quality Assurance leads the site's independent Quality Assurance organization,… more
    Gilead Sciences, Inc. (11/14/25)
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  • Senior Director - Gene Therapy Medical…

    Lilly (Indianapolis, IN)
    …with internal business partners including clinical teams, commercial teams, legal, regulatory affairs , ethics and compliance, and other relevant functions. ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...life better for people around the world. The Senior Director of Gene Therapy Medical Affairs will… more
    Lilly (11/06/25)
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  • Director , Supply Chain Clinical Supply…

    Catalent Pharma Solutions (Philadelphia, PA)
    …successful candidate will work closely with Clinical Operations, Quality Assurance, Regulatory Affairs , and the Program Management team. Strong cross-functional ... **Job Description** We are seeking a ** Director in** **Clinical Supply Chain** to be part...offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us… more
    Catalent Pharma Solutions (10/29/25)
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  • Executive Director , Therapeutic Areas

    Taiho Oncology (Princeton, NJ)
    …guidelines. + Partners with the Clinical Development, Product Development, Regulatory Affairs , Commercial, Legal and Finance departments. Education/Certification ... meet the regional MA needs and facilitate development of global medical affairs strategies for an expanding...is preferred. + Direct work experience with US and/or Global Regulatory authorities is highly preferred. +… more
    Taiho Oncology (11/05/25)
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  • Sr Director Process Translation & Execution…

    Lilly (Indianapolis, IN)
    …Process Development, Engineering, Analytical, Quality, Supply Chain and Raw Materials, and Regulatory Affairs . + Represent the PTE team during regulatory ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (11/24/25)
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  • Manager, Regulatory Counsel

    Edwards Lifesciences (Irvine, CA)
    …Surgical Structural Heart), and other Business Unit or Corporate functions such as Regulatory Affairs , Compliance, and others. . Reviewing and advising on a ... to work from home as needed.** **How you'll make an impact:** The Manager, Regulatory Counsel reports to the Senior Director , Regulatory Counsel and… more
    Edwards Lifesciences (11/05/25)
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  • Director , Quality Assurance - Abbott…

    Abbott (Temecula, CA)
    …making. + Builds strategic partnerships with internal stakeholders, including operations, regulatory affairs , R&D, clinical, operations QA, and ensures alignment ... Abbott is a global healthcare leader that helps people live more...Interacts internally and externally with executive level management, outside regulatory agencies, customers, vendors and/or suppliers. **Qualifications** + Bachelor's… more
    Abbott (11/26/25)
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  • Director - Heart Failure Research

    Lilly (Indianapolis, IN)
    …teams, including medicinal chemistry/genetic medicines/bioproducts, toxicology/ADME, bioinformatics, and regulatory affairs , to integrate data and drive ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (11/01/25)
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  • Sr Dir Quality

    Endo International (St. Louis, MO)
    …of 15 years of pharmacuetical industry experience in a Quality Assurance and/or Regulatory Affairs function including experience in manufacturing and control of ... + Minimum 5 years managerial experience in a pharmaceutial quality/ regulatory affairs environment. _Preferred Skills/Qualifications:_ + Previous experience… more
    Endo International (11/12/25)
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