• Senior Manager , CMC Global…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …drug products and drug-device combination products. Ensure compliance with global regulations ( FDA , EMA, ICH, WHO) and anticipate regulatory changes impacting ... strategies for post-approval changes, line extensions, and global harmonization of product registrations. Monitor and implement regulatory updates impacting… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Clinical Product Manager - Medical…

    Oracle (Sacramento, CA)
    …our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical insight into ... for Clinical Evaluation Reports (CERs), including alignment with EU MDR and FDA regulatory requirements. . Oversee usability engineering (IEC 62366), ensuring… more
    Oracle (12/22/25)
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  • Clinical Product Manager - Medical…

    Oracle (Sacramento, CA)
    …our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical insight into ... for Clinical Evaluation Reports (CERs), including alignment with EU MDR and FDA regulatory requirements. . Oversee usability engineering (IEC 62366), ensuring… more
    Oracle (11/25/25)
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  • Manager , Global Product Quality…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** The Manager , Global Product Quality - Controlled Substances is responsible for ensuring that all activities related to controlled substances ... (CGMP) regulations, Otsuka Quality Standards and US/global (if applicable) regulatory requirements. **Key Responsibilities** + Product Oversight: Provide… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Senior Manager , Global Product

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    The Senior Manager , Global Product Quality - Biologics is responsible for managing quality oversight of clinical and commercial products at CMOs under contract ... and transported in a controlled way that is in accordance with regulatory expectations and applicable GMP/GDP quality standards. This role will provide specialized… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Product Innovation Manager

    Unilever (San Francisco, CA)
    …and future acquisitions to come! This position's home company is OLLY.​ THE ROLE: PRODUCT INNOVATION MANAGER Reporting to the Director of Innovation of VMS, you ... opportunity in supporting shape the VMS-Co-Op pipeline. As a Product Innovation Manager , you will play a...science, Chemistry, or related science field + Familiarity with FDA guidelines for dietary supplementation and regulatory more
    Unilever (12/05/25)
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  • Product Manager , Digital Pathology

    Danaher Corporation (Vista, CA)
    …if you also possess previous experience in: + Experience with regulatory landscapes ( FDA , CE, etc.) and clinical product launches. + 5+ years product ... impact. Learn about the Danaher Business System which makes everything possible. As a Product Manager of our Digital Pathology portfolio, you'll sit at the… more
    Danaher Corporation (12/18/25)
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  • Product Manager - Laboratory

    CliniComp (San Diego, CA)
    The Product Manager for Laboratory leads the development and enhancement of our laboratory solutions. The ideal candidate will have a strong background in ... System (LIS) software. Gather and analyze customer needs, industry trends, and regulatory requirements to inform product development; + Collaborate with software… more
    CliniComp (01/08/26)
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  • Sr. Staff Product Manager

    BD (Becton, Dickinson and Company) (San Diego, CA)
    …best self. Become a **maker of possible** with us. **Job Summary:** The Senior Staff Product Manager will be responsible for managing the product lifecycle ... IDNs. **Required Skills/Experience:** + Bachelor's degree required + 7+ Years in a Product Manager role + Strong project management skills required. + Excellent… more
    BD (Becton, Dickinson and Company) (10/15/25)
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  • Senior Manager , Microbiology

    Cordis (Irvine, CA)
    …manufacturing. + Develop and maintain the microbiology strategy in alignment with combination product regulatory requirements ( FDA , EU MDR, ISO). + ... management. The role partners closely with Quality, Manufacturing, R&D, Regulatory , and external contract manufacturers to ensure product...environments. + Strong working knowledge of GMP, ISO 13485, FDA QSR, EU MDR, and combination product more
    Cordis (12/29/25)
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