• Sr. Scientist Clinical Research

    Abbott (Santa Clara, CA)
    …+ Facilitates communication between Sales and Marketing, R&D, Clinical R&D, Regulatory Affairs, Library Services, Product Performance Group (PPG), Quality ... strategy, the development of plans, reports and project deliverables. Interacts with regulatory agencies as needed, and will use their scientific and medical… more
    Abbott (06/21/25)
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  • Lead Clinical Scientist, Product

    Genentech (South San Francisco, CA)
    …at non-reference HA interactions (TC/F2F) and contribute to varied aspects of regulatory submissions. This position is located in San Francisco, CA (US), Boston, ... MA (US), Welwyn (UK), or Basel (CH). Relocation benefits will not be provided. **Who You Are:** **(Required)** + You hold an Advanced Clinical/Science Degree (eg PhD, PharmD, MSN, MPH, etc). + You have 2+ years of clinical development industry experience, in… more
    Genentech (09/06/25)
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  • Principal Quality Engineer - Shockwave Medical

    J&J Family of Companies (Santa Clara, CA)
    …and third-party audits (FDA, FDB, Notified Body, etc.) + Support ongoing Regulatory submission activities and product approval processes. + Participate in ... products are designed and developed in accordance with customer, corporate, and regulatory guidelines as well as working closely with Design and Manufacturing… more
    J&J Family of Companies (09/06/25)
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  • Senior Manager, Statistics

    AbbVie (South San Francisco, CA)
    …Lake County, IL + South San Francisco, CA Responsibilities: + Support regulatory submission and product life-cycle management strategy planning and ... research programs.Independently develop protocols and statistical analysis plans (or product safety analysis plans/integrated summary of safety analysis plans/analysis… more
    AbbVie (06/24/25)
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  • Senior Principal Scientist, Clinical Research

    Abbott (Sylmar, CA)
    …etc) and outside (R&D, strategic marketing, Clinical R&D, Quality Engineering, Product Performance Group, Risk Management) clinical- regulatory organization, and ... and cross-functional teams in order to develop clinical strategy. Interacts with regulatory agencies as needed, and will use their scientific and medical knowledge… more
    Abbott (08/08/25)
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  • Sr. Manager, Project Management

    Charles Schwab (San Francisco, CA)
    …of the business and include ETF, MF or separately managed account launches, product enhancements, implementation of new regulatory requirements, among a variety ... of the initiative. In addition to traditional project management, the SAM Product and Business Implementation team members facilitate the Product Development… more
    Charles Schwab (08/28/25)
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  • Mechanical Engineer V

    Applied Materials (Santa Clara, CA)
    …disciplines within the function **Business Expertise** + Anticipates business and regulatory issues; recommends product , process or service improvements ... develops and implements concepts for range of significantly complex product issues and engineering solutions Technically lead and/or execute engineering… more
    Applied Materials (08/07/25)
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  • Lead Mechanical Engineer V - (E5)

    Applied Materials (Santa Clara, CA)
    …disciplines within the function **Business Expertise** + Anticipates business and regulatory issues; recommends product , process or service improvements ... develops and implements concepts for range of significantly complex product issues and engineering solutions Technically lead and/or execute engineering… more
    Applied Materials (08/07/25)
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  • Senior Global Trade Compliance Manager

    Oura (San Francisco, CA)
    …trade initiatives, including tariff mitigation strategies, duty savings opportunities, and regulatory planning. + Own product classification, restricted party ... screening, and import/export documentation to ensure regulatory compliance and data accuracy. + Lead trade recordkeeping processes to meet retention requirements… more
    Oura (09/06/25)
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  • QA Document Control Specialist

    Astrix Technology (Los Angeles, CA)
    …+ Manage records, logbooks, certificates, and archival processes + Create/revise product labels and specifications + Support regulatory /customer audits and ... document control activities to ensure compliance with GMP and regulatory requirements. Responsibilities include reviewing, processing, and releasing controlled… more
    Astrix Technology (08/28/25)
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