• CMC Regulatory Affairs

    Parexel (Olympia, WA)
    …motivated professional to join our Global Regulatory Affairs team as a CMC Regulatory Affairs Senior /Consultant. This role is critical to ensure ... contingency plans for CMC -related scenarios * Represent CMC Regulatory Affairs in cross-functional...for a Consultant level role, 7+ years for a Senior Consultant * Proven success in preparing regulatory more
    Parexel (10/11/25)
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  • Senior Regulatory Affairs

    Parexel (Olympia, WA)
    …development and approved programs, helping to shape the future of life-saving therapies. As a ** CMC Regulatory Affairs Senior Associate** , you will play ... scientific discipline (advanced degree preferred). + 4+ years of experience in CMC Regulatory Affairs within the pharmaceutical or biotechnology industry. +… more
    Parexel (10/11/25)
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  • Senior Principal Regulatory

    Bausch + Lomb (Olympia, WA)
    …in assigned due diligence activities for business development and acquisitions. + Lead all CMC regulatory activities for IND, NDA, ANDA, and BLA submissions. + ... Bachelor degree or equivalent, Master degree preferred + Minimum of 8 years in Regulatory Affairs or relevant experience in a regulated environment + Ability to… more
    Bausch + Lomb (09/06/25)
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  • Senior Program Officer, Regulatory

    Bill and Melinda Gates Foundation (Seattle, WA)
    …with the Africa Regional Office, was established at end of 2021. Your Role As a Senior Program Officer, Regulatory Affairs , you will report to the Deputy ... solver, trusted business partner, and subject matter expert in regulatory affairs , especially European regulatory ...+ Work within a team of equally dedicated and senior regulatory experts responsible for the various… more
    Bill and Melinda Gates Foundation (10/10/25)
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  • Senior Regulatory Affairs

    Parexel (Olympia, WA)
    **Join Parexel as a Regulatory Affairs Strategy Lead** Are you a strategic thinker with a passion for navigating the complex world of global regulatory ... plans? If so, we'd love to connect. We're seeking Regulatory Affairs Strategy Leads who will be...programs from early development through approval * Coordinate cross-functional regulatory activities ( CMC , nonclinical, clinical) to meet… more
    Parexel (10/11/25)
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  • Senior Principal Regulatory

    Bausch + Lomb (Olympia, WA)
    …strategies across CMC and clinical/non-clinical, labeling, adpromo domains + Lead all CMC regulatory activities for IND, NDA and ANDA submissions and OTC ... or equivalent; Master's degree preferred + Minimum of 8 years in Regulatory Affairs with experience in the consumer product (Rx/OTC, OTC Monograph, Nutritional,… more
    Bausch + Lomb (09/06/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Olympia, WA)
    …seeking a dynamic, highly motivated, and experienced individual for the position of **Director Regulatory Affairs ** . The Director is part of the Global ... Regulatory Affairs (GRA) team based in the...collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, clinical protocols/study reports,… more
    Sumitomo Pharma (09/09/25)
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  • Senior Manager, Global Regulatory

    Otsuka America Pharmaceutical Inc. (Olympia, WA)
    …with 5+ years' experience or Master's degree with 2 years' experience in regulatory affairs or related areas (eg, clinical development, project management, ... needed. - Works collaboratively with members of the global regulatory team (GRL, regional leads, CMC -RA, labeling,...the global regulatory team (GRL, regional leads, CMC -RA, labeling, medical writing, regulatory operations, etc.)… more
    Otsuka America Pharmaceutical Inc. (08/22/25)
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  • Senior Scientist, Gene Delivery and Editing…

    Bristol Myers Squibb (Seattle, WA)
    …for GMP manufacturing + Expertise in late-stage biologics PD + Working knowledge of regulatory affairs as they relate to biologics and ATMPs + Working knowledge ... their personal lives. Read more: careers.bms.com/working-with-us . **Job Description** The Senior Scientist will join the Gene Delivery and Editing Process… more
    Bristol Myers Squibb (10/10/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Olympia, WA)
    …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... drug substance and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols and timelines,… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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